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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure t
BEE®PLIF cages have been specially adapted to suit the local anatomy to ensure the operative outcome to the greatest extent possible. BEE®PLIF cages are made of titanium alloy in accordance with ASTM F3001 and are produced in an additive manufacturing process. The implants are available in various heights, lengths and lordosis angles. The cranial and caudal side of the implant is rough to achieve a good degree of anchoring of the implant.