Other products from "ADDIVATION MEDICAL, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 B804AOCS61261 AOCS6126 Cervical Spine Interbody Device. 12 x 14mm footprint, 6mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
2 B804AOCS61491 AOCS6149 Cervical Spine Interbody Device. 14 x 16mm footprint, 9mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
3 B804AOCS61481 AOCS6148 Cervical Spine Interbody Device. 14 x 16mm footprint, 8mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
4 B804AOCS61471 AOCS6147 Cervical Spine Interbody Device. 14 x 16mm footprint, 7mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
5 B804AOCS61461 AOCS6146 Cervical Spine Interbody Device. 14 x 16mm footprint, 6mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
6 B804AOCS61451 AOCS6145 Cervical Spine Interbody Device. 14 x 16mm footprint, 5mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
7 B804AOCS61421 AOCS6142 Cervical Spine Interbody Device. 14 x 16mm footprint, 12mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
8 B804AOCS61401 AOCS6140 Cervical Spine Interbody Device. 14 x 16mm footprint, 10mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
9 B804AOCS61291 AOCS6129 Cervical Spine Interbody Device. 12 x 14mm footprint, 9mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
10 B804AOCS61281 AOCS6128 Cervical Spine Interbody Device. 12 x 14mm footprint, 8mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
11 B804AOCS61271 AOCS6127 Cervical Spine Interbody Device. 12 x 14mm footprint, 7mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
12 B804AOCS61251 AOCS6125 Cervical Spine Interbody Device. 12 x 14mm footprint, 5mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
13 B804AOCS61221 AOCS6122 Cervical Spine Interbody Device. 12 x 14mm footprint, 12mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
14 B804AOCS61211 AOCS6121 Cervical Spine Interbody Device. 12 x 14mm footprint, 11mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
15 B804AOCS61201 AOCS6120 Cervical Spine Interbody Device. 12 x 14mm footprint, 10mm height, 6 degrees lordosis. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 Addivation Medical Cervical Interbody Device
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00813210020856 CIC2-10-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
2 00813210020849 CIC2-09-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
3 00813210020832 CIC2-08-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
4 00813210020788 CIC2-A743 Expander VariLift-C WENZEL SPINE, INC.
5 00813210020771 CIC2-A742 Retainer VariLift-C WENZEL SPINE, INC.
6 00813210020764 CIC2-A741 Inserter VariLift-C WENZEL SPINE, INC.
7 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
8 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
9 00813210020252 CIC1-A747 Removal Screwdriver VariLift-C WENZEL SPINE, INC.
10 00813210020221 CIC1-A743 Expansion Wrench VariLift-C WENZEL SPINE, INC.
11 00813210020214 CIC1-A742 Locking Wrench VariLift-C WENZEL SPINE, INC.
12 00813210020207 CIC1-A741 Insertion Wrench VariLift-C WENZEL SPINE, INC.
13 00813210020061 CIC1-9.0-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
14 00813210020054 CIC1-7.5-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
15 00813210020047 CIC1-9.0-12-BP The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
16 00813210020030 CIC1-7.5-12-BP The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
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