Other products from "EVOLUTION SPINE LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00195860016398 101-A013 101-A013 DTS DRILL 14mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
2 00195860016435 101-A005 101-A005 DTS GUIDE 9mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
3 00195860016428 101-A016 101-A016 DTS DRILL 20mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
4 00195860016374 101-A011 101-A011 DTS DRILL 10mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
5 00195860016367 101-A010 101-A010 INLINE INSERTER LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
6 00195860016350 101-A009 101-A009 INLINE INSERTER DRAWBAR LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
7 00195860016343 101-A008 101-A008 DTS GUIDE 12mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
8 00195860016336 101-A007 101-A007 DTS GUIDE 11mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
9 00195860016329 101-A006 101-A006 DTS GUIDE 10mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
10 00195860010211 CP755 CP755 75mm 5 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
11 00195860010204 CP844 CP844 84mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
12 00195860010198 CP804 CP804 80mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
13 00195860010181 CP764 CP764 76mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
14 00195860010174 CP724 CP724 72mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
15 00195860010167 CP684 CP684 68mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
16 00195860010150 CP644 CP644 64mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
17 00195860010143 CP604 CP604 60mm 4 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
18 00195860010082 CP623 CP623 62mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
19 00195860010075 CP593 CP593 59mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
20 00195860010068 CP563 CP563 56mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
21 00195860010051 CP533 CP533 53mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
22 00195860010044 CP503 CP503 50mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
23 00195860010037 CP473 CP473 47mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
24 00195860010020 CP443 CP443 44mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
25 00195860010013 CP413 CP413 41mm 3 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
26 00195860010006 CP482 CP482 48mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
27 00195860009994 CP452 CP452 45mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
28 00195860009987 CP422 CP422 42mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
29 00195860009970 CP392 CP392 39mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
30 00195860009963 CP362 CP362 36mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
31 00195860009956 CP332 CP332 33mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
32 00195860009949 CP302 CP302 30mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
33 00195860009932 CP282 CP282 28mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
34 00195860009925 CP262 CP262 26mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
35 00195860009918 CP242 CP242 24mm 2 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
36 00195860009901 CP281 CP281 28mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
37 00195860009895 CP261 CP261 26mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
38 00195860009888 CP241 CP241 24mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
39 00195860009871 CP221 CP221 22mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
40 00195860009864 CP201 CP201 20mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
41 00195860009857 CP181 CP181 18mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
42 00195860009840 CP161 CP161 16mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
43 00195860009833 CP141 CP141 14mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
44 00195860009826 CP121 CP121 12mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
45 00195860009819 CP101 CP101 10mm 1 Level Plate KWQ Appliance, fixation, spinal intervertebral body 2 Skye Cervical Plate System
46 00195860016411 101-A015 101-A015 DTS DRILL 18mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
47 00195860016404 101-A014 101-A014 DTS DRILL 16mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
48 00195860016381 101-A012 101-A012 DTS DRILL 12mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
49 00195860016305 101-A004 101-A004 DTS GUIDE 8mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
50 00195860016299 101-A003 101-A003 DTS GUIDE 7mm LXH Orthopedic manual surgical instrument 1 EMERGE Micro Anterior Cervical Plate System
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