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primaLOK FF 25mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle.

SET OF 10 ANCHOR BOLTS, LENGTH 25MM, ACCESSORY OF MICRODEEP DEPTH ELECTRODE

Hemapatch Knitted Collagen Coated Vascular Patch

Hemagard Patch Knitted Collagen Coated Vascular Patch

Hemagard Patch Knitted Collagen Coated Vascular Patch

Hemagard Patch Knitted Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Ultrathin Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Collagen Coated Vascular Patch

Hemagard Carotid Patch Knitted Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Collagen Coated Vascular Patch

Hemacarotidpatch Knitted Collagen Coated Vascular Patch

16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.

14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.

12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.

10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation