Other products from "LIFE SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00190837003630 80-3830-0617 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
2 00190837003678 80-3830-1217 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
3 00190837003661 80-3830-1215 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
4 00190837003654 80-3830-1213 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
5 00190837003647 80-3830-1211 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
6 00190837003623 80-3830-0615 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
7 00190837003616 80-3830-0613 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
8 00190837003609 80-3830-0611 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
9 00190837003593 80-3226-1217 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
10 00190837003586 80-3226-1215 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
11 00190837003579 80-3226-1213 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
12 00190837003562 80-3226-1211 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
13 00190837003555 80-3226-0617 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
14 00190837003548 80-3226-0615 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
15 00190837003531 80-3226-0613 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
16 00190837003524 80-3226-0611 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
17 00190837003517 80-155-30 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
18 00190837003500 80-155-25 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
19 00190837003494 80-155-20 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar 2 Dyna-Link Stand-Alone Anterior Lumbar System
20 00190837137106 132-2314-2 PEK Spinous Process Plate 2 Aileron TRX
21 00190837137090 132-2308-2 PEK Spinous Process Plate 2 Aileron TRX
22 00190837098230 132-1-131 132-1-131 PEK Spinous process plate 2 Aileron Static
23 00190837094607 113-726 113-726 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
24 00190837094591 113-547 113-547 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
25 00190837094034 113-1444 113-1444 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
26 00190837093846 113-1744 113-1744 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
27 00190837093839 113-1743 113-1743 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
28 00190837093822 113-1742 113-1742 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
29 00190837093815 113-1741 113-1741 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
30 00190837093808 113-1740 113-1740 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
31 00190837093792 113-1739 113-1739 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
32 00190837093785 113-1738 113-1738 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
33 00190837093778 113-1737 113-1737 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
34 00190837093761 113-1736 113-1736 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
35 00190837093754 113-1735 113-1735 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
36 00190837093747 114-1444 114-1444 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
37 00190837093730 113-1443 113-1443 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
38 00190837093723 113-1442 113-1442 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
39 00190837093716 113-1441 113-1441 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
40 00190837093709 113-1440 113-1440 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
41 00190837093693 113-1439 113-1439 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
42 00190837093686 113-1438 113-1438 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
43 00190837093679 113-1437 113-1437 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
44 00190837093662 113-1436 113-1436 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
45 00190837093655 113-1435 113-1435 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
46 00190837093648 113-1044 113-1044 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
47 00190837093631 113-1043 113-1043 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
48 00190837093624 113-1042 113-1042 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
49 00190837093617 113-1038 113-1038 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
50 00190837093600 113-1036 113-1036 ODP Intervertebral fusion device with bone graft, cervical 2 Plateau C
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00814008022557 AC-612-L 14X16 12mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
2 00814008022540 AC-611-L 14X16 11mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
3 00814008022533 AC-610-L 14X16 10mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
4 00814008022526 AC-609-L 14X16 9mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
5 00814008022519 AC-608-L 14X16 8mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
6 00814008022502 AC-607-L 14X16 7mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
7 00814008022496 AC-606-L 14X16 6mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
8 00814008022489 AC-605-L 14X16 5mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
9 00814008022472 AC-012-L 14X16 12mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
10 00814008022465 AC-011-L 14X16 11mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
11 00814008022458 AC-010-L 14X16 10mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
12 00814008022441 AC-009-L 14X16 9mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
13 00814008022434 AC-008-L 14X16 8mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
14 00814008022427 AC-007-L 14X16 7mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
15 00814008022410 AC-006-L 14X16 6mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00814008022403 AC-005-L 14X16 5mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008022397 AC-612-S 12X14 12mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008022380 AC-611-S 12X14 11mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008022373 AC-610-S 12X14 10mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008022366 AC-609-S 12X14 9mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008022359 AC-608-S 12X14 8mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00814008022342 AC-607-S 12X14 7mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00814008022335 AC-606-S 12X14 6mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00814008022328 AC-605-S 12X14 5mm 6 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00814008022311 AC-012-S 12X14 12mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00814008022304 AC-011-S 12X14 11mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00814008022298 AC-010-S 12X14 10mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00814008022281 AC-009-S 12X14 9mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00814008022274 AC-008-S 12X14 8mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00814008022267 AC-007-S 12X14 7mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
31 00814008022250 AC-006-S 12X14 6mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
32 00814008022243 AC-005-S 12X14 5mm 0 Degree ACIF - Anterior Cervical Interbody Fusion System NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 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.
34 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.
35 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.
36 00813210020788 CIC2-A743 Expander VariLift-C WENZEL SPINE, INC.
37 00813210020771 CIC2-A742 Retainer VariLift-C WENZEL SPINE, INC.
38 00813210020764 CIC2-A741 Inserter VariLift-C WENZEL SPINE, INC.
39 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
40 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
41 00813210020252 CIC1-A747 Removal Screwdriver VariLift-C WENZEL SPINE, INC.
42 00813210020221 CIC1-A743 Expansion Wrench VariLift-C WENZEL SPINE, INC.
43 00813210020214 CIC1-A742 Locking Wrench VariLift-C WENZEL SPINE, INC.
44 00813210020207 CIC1-A741 Insertion Wrench VariLift-C WENZEL SPINE, INC.
45 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.
46 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.
47 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.
48 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.
49 00812998044399 CSTS-000022 CSTS-000022 4WEB Medical 4WEB MEDICAL
50 00812998044382 CSTS-000021 CSTS-000021 4WEB Medical 4WEB MEDICAL