Other products from "GS MEDICAL CO., LTD."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08806395497935 GS142-0803 GS142-0803 Screw Extractor LXH Orthopedic Manual Surgical Instrument 1 CASSIOPEIA ACP
2 08806395478828 GS148-2650 GS148-2650 Ring Curette, 10mm Straight HTF Curette 1 AnyPlus®
3 08806395403486 GS110-2316 GS110-2316 Set Screw Starter HWD Starter, Bone Screw 1 GSS™ and AnyPlus®
4 08806395403127 GS110-1526 GS110-1526 French Rod Bender HXW Bender 1 GSS™ and AnyPlus®
5 08806395453207 2711-7540 2711-7540 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NBK,KWQ,KWP,MNH,MNI System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Sp System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 AnyPlus Spinal Fixation System
6 08806395453191 2711-7535 2711-7535 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. MNI,MNH,KWP,KWQ,NBK Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer 2 AnyPlus Spinal Fixation System
7 08806395453184 2711-7530 2711-7530 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NBK,KWQ,KWP,MNH,MNI System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Sp System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 AnyPlus Spinal Fixation System
8 08806395453177 2711-7525 2711-7525 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. MNI,MNH,KWP,KWQ,NBK Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer 2 AnyPlus Spinal Fixation System
9 08806395453160 2711-7000 2711-7000 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NBK,KWQ,KWP,MNH,MNI System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Sp System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 AnyPlus Spinal Fixation System
10 08806395453153 2711-7095 2711-7095 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. MNI,MNH,KWP,KWQ,NBK Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Interlaminal,Appliance, Fixation, Spinal Intervertebral Body,System,Test,(Ihc),Tumor Marker,Monitoring,Bladder Cancer 2 AnyPlus Spinal Fixation System
11 08809237298486 GS0162-1150-M0 GS0162-1150-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
12 08809237298479 GS0162-1145-M0 GS0162-1145-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
13 08809237298462 GS0162-1140-M0 GS0162-1140-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
14 08809237298455 GS0162-1135-M0 GS0162-1135-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
15 08809237298448 GS0162-1130-M0 GS0162-1130-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. MNI,MNH,KWQ,KWP,NKB Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Ap Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 AnyPlus Spinal Fixation System
16 08809237298431 GS0162-1125-M0 GS0162-1125-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
17 08809237298424 GS0162-1120-M0 GS0162-1120-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
18 08809237298417 GS0162-1115-M0 GS0162-1115-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
19 08809237298400 GS0162-1110-M0 GS0162-1110-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
20 08809237298394 GS0162-1105-M0 GS0162-1105-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
21 08809237298387 GS0162-1100-M0 GS0162-1100-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
22 08809237298370 GS0162-1095-M0 GS0162-1095-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
23 08809237298363 GS0162-1090-M0 GS0162-1090-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
24 08809237298356 GS0162-1085-M0 GS0162-1085-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
25 08809237298349 GS0162-1080-M0 GS0162-1080-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. KWQ,KWP,MNH,MNI,NKB Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease 2 AnyPlus Spinal Fixation System
26 08809237298332 GS0162-1075-M0 GS0162-1075-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
27 08809237298325 GS0162-1070-M0 GS0162-1070-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
28 08809237298318 GS0162-1065-M0 GS0162-1065-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
29 08809237298301 GS0162-1060-M0 GS0162-1060-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
30 08809237298295 GS0162-1055-M0 GS0162-1055-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
31 08809237298288 GS0162-1050-M0 GS0162-1050-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
32 08809237298271 GS0162-1045-M0 GS0162-1045-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
33 08809237298264 GS0162-1040-M0 GS0162-1040-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
34 08809237298257 GS0162-0150-M0 GS0162-0150-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
35 08809237298240 GS0162-0145-M0 GS0162-0145-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
36 08809237298233 GS0162-0140-M0 GS0162-0140-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
37 08809237298226 GS0162-0135-M0 GS0162-0135-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
38 08809237298219 GS0162-0130-M0 GS0162-0130-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
39 08809237298202 GS0162-0125-M0 GS0162-0125-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
40 08809237298196 GS0162-0120-M0 GS0162-0120-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
41 08809237298189 GS0162-0115-M0 GS0162-0115-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
42 08809237298172 GS0162-0110-M0 GS0162-0110-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
43 08809237298165 GS0162-0105-M0 GS0162-0105-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
44 08809237298158 GS0162-0100-M0 GS0162-0100-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
45 08809237298141 GS0162-0095-M0 GS0162-0095-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
46 08809237298134 GS0162-0090-M0 GS0162-0090-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
47 08809237298127 GS0162-0085-M0 GS0162-0085-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
48 08809237298110 GS0162-0080-M0 GS0162-0080-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
49 08809237298103 GS0162-0075-M0 GS0162-0075-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
50 08809237298097 GS0162-0070-M0 GS0162-0070-M0 The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and c The AnyPlus Spinal Fixation System consists of various hooks, screws, rods and connectors and is intended to create a rigid spinal construct. The components are manufactured from Ti6AI4V ELI according to ISO 5832-3 and ASTM F-136. The screws are available from 4.0 to 10.5mm diameters with lengths ranging from 20 to 100mm (Length does not include the screw head). Specialized instruments are available for the application and removal of the Anypluss Spinal Fixation System. AnyPlus Spinal Fixation System are non-cervical spinal fixation devices intended for use as posterior pedicle screw fixation systems (T1 -S2), a posterior hook fixation system (T 1-5), or as a anterolateral fixation system (T8-L_5). All components in the system are limited to skeletally mature patients. System components are to be used for immobilization and stabilization of the spine as an adjunct to fusion. These devices are indicated for all of the following indications regardless of the intended use: degenerative disc disease (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fracture or dislocation), deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis, Scheuermann's Disease), tumor, stenosis, pseudoarthrosis, and failed previous fusion. NKB,MNI,MNH,KWQ,KWP Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spina Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal 2 AnyPlus Spinal Fixation System
Other products with the same Product Codes "KWQ, MNH, MNI, NKB"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04719873024841 43566560 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=60 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
2 04719873024834 43566555 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=55 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
3 04719873024827 43566550 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=50 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
4 04719873024810 43566545 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
5 04719873024803 43566540 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=40 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
6 04719873024797 43566535 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
7 04719873024780 43566530 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.5 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
8 04719873024773 43566055 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=55 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
9 04719873024766 43566050 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=50 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
10 04719873024759 43566045 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
11 04719873024742 43566040 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=40 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
12 04719873024735 43566035 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
13 04719873024728 43566030 Polyaxial Reduction Pedicle Screw, Cannulated ø=6.0 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
14 04719873024711 43565550 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.5 L=50 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
15 04719873024704 43565545 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.5 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
16 04719873024698 43565540 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.5 L=40 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
17 04719873024681 43565535 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.5 L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
18 04719873024674 43565530 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.5 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
19 04719873024667 43565045 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.0 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
20 04719873024650 43565040 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.0 L=40 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
21 04719873024643 43565035 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.0 L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
22 04719873024636 43565030 Polyaxial Reduction Pedicle Screw, Cannulated ø=5.0 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
23 04719873024254 43555530 Polyaxial Reduction Pedicle Screw ø=5.5 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
24 04719873024247 43555045 Polyaxial Reduction Pedicle Screw ø=5.0 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
25 04719873024223 43555035 Polyaxial Pedicle Screw ø=5.0 / L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. WILTROM SPINAL FIXATION SYSTEM WILTROM CO., LTD.
26 04719873024216 43555030 Polyaxial Pedicle Screw ø=5.0 / L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. WILTROM SPINAL FIXATION SYSTEM WILTROM CO., LTD.
27 04719873024209 43547570 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=70 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
28 04719873024193 43547565 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=65 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
29 04719873024186 43547560 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=60 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
30 04719873024179 43547555 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=55 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
31 04719873024162 43547550 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=50 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
32 04719873024155 43547545 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=45 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
33 04719873024148 43547540 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=40 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
34 04719873024131 43547535 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=35 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
35 04719873024124 43547530 Polyaxial Pedicle Screw, Cannulated ø=7.5 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
36 04719873023790 43545030 Polyaxial Pedicle Screw, Cannulated ø=5.0 L=30 The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link conn The Wiltrom Spinal Fixation System is comprised of screws, rods, cross-link connector and associated surgical instruments thatallow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. The Wiltrom SpinalFixation System is designed to be used to stabilize the vertebrae through a posterior approach. The Wiltrom spinal implants aremade of Ti-6Al-4V ELI material which complies with ISO 5832-3 and ASTM F136. Wiltrom Spinal Fixation System is provided nonsterile,and the implants are for single use only. Wiltrom Spinal Fixation System WILTROM CO., LTD.
37 04718251509123 662-8060 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
38 04718251509116 662-8055 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
39 04718251509109 662-8050 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
40 04718251509093 662-8045 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
41 04718251509086 662-8040 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
42 04718251509079 662-8035 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
43 04718251509062 662-8030 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
44 04718251509055 662-7560 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
45 04718251509048 662-7555 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
46 04718251509031 662-7550 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
47 04718251509024 662-7545 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
48 04718251509017 662-7540 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
49 04718251509000 662-7535 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.
50 04718251508997 662-7530 Pedicle Long Screw Facilis™ Spinal System BAUI BIOTECH CO. LTD.