Other products from "ORTHO DEVELOPMENT CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00822409114702 C-1755-81 Uni Femoral Drill-Thru Trial Size 8 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
2 00822409114696 C-1755-71 Uni Femoral Drill-Thru Trial Size 7 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
3 00822409114689 C-1755-61 Uni Femoral Drill-Thru Trial Size 6 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
4 00822409114672 C-1755-51 Uni Femoral Drill-Thru Trial Size 5 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
5 00822409114665 C-1755-41 Uni Femoral Drill-Thru Trial Size 4 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
6 00822409114658 C-1755-31 Uni Femoral Drill-Thru Trial Size 3 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
7 00822409114641 C-1755-21 Uni Femoral Drill-Thru Trial Size 2 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
8 00822409114634 C-1755-11 Uni Femoral Drill-Thru Trial Size 1 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
9 00822409114795 C-1754 Uni Drill-Thru Femoral Trial Lug Drill HTW BIT, DRILL 1 n/a
10 00822409114368 C-1683 Posterior Referencing Sizer with Adjustable Boom LXH Orthopedic manual surgical instrument 1 n/a
11 00822409114351 C-1762-02 Uni Tibial Cut Guide 3 Degree Right Uncaptured LXH Orthopedic manual surgical instrument 1 n/a
12 00822409114344 C-1762-01 Uni Tibial Cut Guide 3 Degree Left Uncaptured LXH Orthopedic manual surgical instrument 1 n/a
13 00822409114771 C-1755-72 Uni Femoral Drill-Thru Trial Size 7 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
14 00822409114764 C-1755-62 Uni Femoral Drill-Thru Trial Size 6 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
15 00822409114726 C-1755-22 Uni Femoral Drill-Thru Trial Size 2 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
16 00822409114719 C-1755-12 Uni Femoral Drill-Thru Trial Size 1 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
17 00822409114733 C-1755-32 Uni Femoral Drill-Thru Trial Size 3 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
18 00822409114757 C-1755-52 Uni Femoral Drill-Thru Trial Size 5 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
19 00822409114740 C-1755-42 Uni Femoral Drill-Thru Trial Size 4 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
20 00822409114788 C-1755-82 Uni Femoral Drill-Thru Trial Size 8 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
21 00822409114337 C-1761-02 Uni Tibial Cut Guide 3° Right Captured LXH Orthopedic manual surgical instrument 1 n/a
22 00822409114320 C-1761-01 Uni Tibial Cut Guide 3° Left Captured LXH Orthopedic manual surgical instrument 1 n/a
23 00822409114245 C-1752-03 Uni Shim, 3 mm LXH Orthopedic manual surgical instrument 1 n/a
24 00822409114238 C-1752-02 Uni Shim, 2 mm LXH Orthopedic manual surgical instrument 1 n/a
25 00822409114207 C-1760 Uni Alignment Rod Adapter LXH Orthopedic manual surgical instrument 1 n/a
26 00822409114191 C-1759-15 Uni Spacer Block 15mm x 22mm LXH Orthopedic manual surgical instrument 1 n/a
27 00822409114184 C-1759-14 Uni Spacer Block 14mm x 21mm LXH Orthopedic manual surgical instrument 1 n/a
28 00822409114177 C-1759-13 Uni Spacer Block 13mm x 20mm LXH Orthopedic manual surgical instrument 1 n/a
29 00822409114160 C-1759-12 Uni Spacer Block 12mm x 19mm LXH Orthopedic manual surgical instrument 1 n/a
30 00822409114153 C-1759-11 Uni Spacer Block 11mm x 18mm LXH Orthopedic manual surgical instrument 1 n/a
31 00822409114146 C-1759-10 Uni Spacer Block 10mm x 17mm LXH Orthopedic manual surgical instrument 1 n/a
32 00822409114139 C-1759-09 Uni Spacer Block 9mm x 16mm LXH Orthopedic manual surgical instrument 1 n/a
33 00822409114122 C-1759-08 Uni Spacer Block 8mm x 15mm LXH Orthopedic manual surgical instrument 1 n/a
34 00822409114115 C-1756 Slim I/M Sleeve Adapter LXH Orthopedic Manual Surgical Instrument 1 n/a
35 00822409114108 C-1749-52 Uni Femoral Monoblock Distal Cut Guide R 13 x 5 LXH Orthopedic manual surgical instrument 1 n/a
36 00822409114092 C-1749-42 Uni Femoral Monoblock Distal Cut Guide R 12 x 5 LXH Orthopedic manual surgical instrument 1 n/a
37 00822409114085 C-1749-32 Uni Femoral Monoblock Distal Cut Guide R 11 x 6 LXH Orthopedic manual surgical instrument 1 n/a
38 00822409114078 C-1749-22 Uni Femoral Monoblock Distal Cut Guide R 10 x 7 LXH Orthopedic manual surgical instrument 1 n/a
39 00822409114061 C-1749-12 Uni Femoral Monoblock Distal Cut Guide R 9 x 8 LXH Orthopedic manual surgical instrument 1 n/a
40 00822409114054 C-1749-02 Uni Femoral Monoblock Distal Cut Guide R 9 x 7 LXH Orthopedic manual surgical instrument 1 n/a
41 00822409114047 C-1749-51 Uni Femoral Monoblock Distal Cut Guide L 13 x 5 LXH Orthopedic manual surgical instrument 1 n/a
42 00822409114030 C-1749-41 Uni Femoral Monoblock Distal Cut Guide L 12 x 5 LXH Orthopedic manual surgical instrument 1 n/a
43 00822409110940 C-1645 Ratcheting Handle LXH Orthopedic manual surgical instrument 1 n/a
44 00822409114023 C-1749-31 Uni Femoral Monoblock Distal Cut Guide L 11 x 6 LXH Orthopedic manual surgical instrument 1 n/a
45 00822409114016 C-1749-21 Uni Femoral Monoblock Distal Cut Guide L 10 x 7 LXH Orthopedic manual surgical instrument 1 n/a
46 00822409114009 C-1749-11 Uni Femoral Monoblock Distal Cut Guide L 9 x 8 LXH Orthopedic manual surgical instrument 1 n/a
47 00822409113996 C-1749-01 Uni Femoral Monoblock Distal Cut Guide L 9 x 7 LXH Orthopedic manual surgical instrument 1 n/a
48 00822409113989 C-1751 Uni Stabilizer Block Curved 9mm LXH Orthopedic manual surgical instrument 1 n/a
49 00822409113972 C-1750 Uni Stabilizer Block Flat 9mm LXH Orthopedic manual surgical instrument 1 n/a
50 00822409113965 C-1344-38 A/P Sizing Guide Left Paddle LXH Orthopedic manual surgical instrument 1 n/a
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