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 Code "LXH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00844856098497 67119-109 Cervical Square Lordotic Small Trial, Smooth, 9mm Cortical Allograft ALPHATEC SPINE, INC.
2 00844856098480 67119-108 Cervical Square Lordotic Small Trial, Smooth, 8mm Cortical Allograft ALPHATEC SPINE, INC.
3 00844856098473 67119-107 Cervical Square Lordotic Small Trial, Smooth, 7mm Cortical Allograft ALPHATEC SPINE, INC.
4 00844856098466 67119-106 Cervical Square Lordotic Small Trial, Smooth, 6mm Cortical Allograft ALPHATEC SPINE, INC.
5 00844856098459 67119-105 Cervical Square Lordotic Small Trial, Smooth, 5mm Cortical Allograft ALPHATEC SPINE, INC.
6 00844856098442 67119-009 Cervical Square Parallel Small Trial, Smooth, 9mm Cortical Allograft ALPHATEC SPINE, INC.
7 00844856098435 67119-008 Cervical Square Parallel Small Trial, Smooth, 8mm Cortical Allograft ALPHATEC SPINE, INC.
8 00844856098428 67119-007 Cervical Square Parallel Small Trial, Smooth, 7mm Cortical Allograft ALPHATEC SPINE, INC.
9 00844856098411 67119-006 Cervical Square Parallel Small Trial, Smooth, 6mm Cortical Allograft ALPHATEC SPINE, INC.
10 00844856098404 67119-005 Cervical Square Parallel Small Trial, Smooth, 5mm Cortical Allograft ALPHATEC SPINE, INC.
11 00844856098381 67118-110 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 10MM ATEC Biologics ALPHATEC SPINE, INC.
12 00844856098374 67118-109 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 9MM ATEC Biologics ALPHATEC SPINE, INC.
13 00844856098367 67118-108 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 8MM ATEC Biologics ALPHATEC SPINE, INC.
14 00844856098350 67118-107 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 7MM ATEC Biologics ALPHATEC SPINE, INC.
15 00844856098343 67118-106 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 6MM ATEC Biologics ALPHATEC SPINE, INC.
16 00844856098336 67118-105 LORDOTIC DENSE CANCELLOUS TRIAL, RASPING, 5MM ATEC Biologics ALPHATEC SPINE, INC.
17 00844856098244 67117-110 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 10MM ATEC Biologics ALPHATEC SPINE, INC.
18 00844856098237 67117-109 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 9MM ATEC Biologics ALPHATEC SPINE, INC.
19 00844856098220 67117-108 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 8MM ATEC Biologics ALPHATEC SPINE, INC.
20 00844856098213 67117-107 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 7MM ATEC Biologics ALPHATEC SPINE, INC.
21 00844856098206 67117-106 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 6MM ATEC Biologics ALPHATEC SPINE, INC.
22 00844856098190 67117-105 LORDOTIC DENSE CANCELLOUS TRIAL, SMOOTH, 5MM ATEC Biologics ALPHATEC SPINE, INC.
23 00844856098107 67116-110 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 10MM ATEC Biologics ALPHATEC SPINE, INC.
24 00844856098091 67116-109 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 9MM ATEC Biologics ALPHATEC SPINE, INC.
25 00844856098084 67116-108 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 8MM ATEC Biologics ALPHATEC SPINE, INC.
26 00844856098077 67116-107 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 7MM ATEC Biologics ALPHATEC SPINE, INC.
27 00844856098060 67116-106 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 6MM ATEC Biologics ALPHATEC SPINE, INC.
28 00844856098053 67116-105 CERVICAL LORDOTIC LARGE TRIAL, RASPING, 5MM ATEC Biologics ALPHATEC SPINE, INC.
29 00844856098039 67116-010 CERVICAL PARALLEL LARGE TRIAL, RASPING, 10MM ATEC Biologics ALPHATEC SPINE, INC.
30 00844856098022 67116-009 CERVICAL PARALLEL LARGE TRIAL, RASPING, 9MM ATEC Biologics ALPHATEC SPINE, INC.
31 00844856098015 67116-008 CERVICAL PARALLEL LARGE TRIAL, RASPING, 8MM ATEC Biologics ALPHATEC SPINE, INC.
32 00844856098008 67116-007 CERVICAL PARALLEL LARGE TRIAL, RASPING, 7MM ATEC Biologics ALPHATEC SPINE, INC.
33 00844856097995 67116-006 CERVICAL PARALLEL LARGE TRIAL, RASPING, 6MM ATEC Biologics ALPHATEC SPINE, INC.
34 00844856097988 67116-005 CERVICAL PARALLEL LARGE TRIAL, RASPING, 5MM ATEC Biologics ALPHATEC SPINE, INC.
35 00844856097964 67115-110 CERVICAL LORDOTIC LARGE TRIAL, 10MM ATEC Biologics ALPHATEC SPINE, INC.
36 00844856097957 67115-109 CERVICAL LORDOTIC LARGE TRIAL, 9MM ATEC Biologics ALPHATEC SPINE, INC.
37 00844856097940 67115-108 CERVICAL LORDOTIC LARGE TRIAL, 8MM ATEC Biologics ALPHATEC SPINE, INC.
38 00844856097933 67115-107 CERVICAL LORDOTIC LARGE TRIAL, 7MM ATEC Biologics ALPHATEC SPINE, INC.
39 00844856097926 67115-106 CERVICAL LORDOTIC LARGE TRIAL, 6MM ATEC Biologics ALPHATEC SPINE, INC.
40 00844856097919 67115-105 CERVICAL LORDOTIC LARGE TRIAL, 5MM ATEC Biologics ALPHATEC SPINE, INC.
41 00844856097896 67115-010 CERVICAL PARALLEL LARGE TRIAL, 10MM ATEC Biologics ALPHATEC SPINE, INC.
42 00844856097889 67115-009 CERVICAL PARALLEL LARGE TRIAL, 9MM ATEC Biologics ALPHATEC SPINE, INC.
43 00844856097872 67115-008 CERVICAL PARALLEL LARGE TRIAL, 8MM ATEC Biologics ALPHATEC SPINE, INC.
44 00844856097865 67115-007 CERVICAL PARALLEL LARGE TRIAL, 7MM ATEC Biologics ALPHATEC SPINE, INC.
45 00844856097858 67115-006 CERVICAL PARALLEL LARGE TRIAL, 6MM ATEC Biologics ALPHATEC SPINE, INC.
46 00844856097841 67115-005 CERVICAL PARALLEL LARGE TRIAL, 5MM ATEC Biologics ALPHATEC SPINE, INC.
47 00844856097834 67114-110 CERVICAL LORDOTIC SMALL TRIAL, RASPING, 10MM ATEC Biologics ALPHATEC SPINE, INC.
48 00844856097827 67114-109 CERVICAL LORDOTIC SMALL TRIAL, RASPING, 9MM ATEC Biologics ALPHATEC SPINE, INC.
49 00844856097810 67114-108 CERVICAL LORDOTIC SMALL TRIAL, RASPING, 8MM ATEC Biologics ALPHATEC SPINE, INC.
50 00844856097803 67114-107 CERVICAL LORDOTIC SMALL TRIAL, RASPING, 7MM ATEC Biologics ALPHATEC SPINE, INC.