Other products from "TYBER MEDICAL LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M695M9654300 M9-65430 M9-65430 HWC Screw, fixation, bone 2 N/A
2 M695M9653950 M9-65395 M9-65395 HWC Screw, fixation, bone 2 N/A
3 M695M9653900 M9-65390 M9-65390 HWC Screw, fixation, bone 2 N/A
4 M695M9653850 M9-65385 M9-65385 HWC Screw, fixation, bone 2 N/A
5 M695M9653800 M9-65380 M9-65380 HWC Screw, fixation, bone 2 N/A
6 M695M9653750 M9-65375 M9-65375 HWC Screw, fixation, bone 2 N/A
7 M695M9653700 M9-65370 M9-65370 HWC Screw, fixation, bone 2 N/A
8 M695M9654580 M9-65458 M9-65458 HWC Screw, fixation, bone 2 N/A
9 M695M9654560 M9-65456 M9-65456 HWC Screw, fixation, bone 2 N/A
10 M695M9654540 M9-65454 M9-65454 HWC Screw, fixation, bone 2 N/A
11 M695M9654520 M9-65452 M9-65452 HWC Screw, fixation, bone 2 N/A
12 M695M9654500 M9-65450 M9-65450 HWC Screw, fixation, bone 2 N/A
13 M695M9654480 M9-65448 M9-65448 HWC Screw, fixation, bone 2 N/A
14 M695M9654460 M9-65446 M9-65446 HWC Screw, fixation, bone 2 N/A
15 M695M9654440 M9-65444 M9-65444 HWC Screw, fixation, bone 2 N/A
16 M695M9654420 M9-65442 M9-65442 HWC Screw, fixation, bone 2 N/A
17 M695M9654400 M9-65440 M9-65440 HWC Screw, fixation, bone 2 N/A
18 M695M9654380 M9-65438 M9-65438 HWC Screw, fixation, bone 2 N/A
19 M695M9654360 M9-65436 M9-65436 HWC Screw, fixation, bone 2 N/A
20 M695M9654340 M9-65434 M9-65434 HWC Screw, fixation, bone 2 N/A
21 M695M9653650 M9-65365 M9-65365 HWC Screw, fixation, bone 2 N/A
22 M695M9653600 M9-65360 M9-65360 HWC Screw, fixation, bone 2 N/A
23 00819917020717 108843612 108843612 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
24 00819917020700 108843611 108843611 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
25 00819917020694 108843610 108843610 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
26 00819917020687 108843609 108843609 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
27 00819917020670 108843608 108843608 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
28 00819917020663 108843607 108843607 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
29 00819917020656 108843606 108843606 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
30 00819917020649 108843605 108843605 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
31 00819917020632 108843512 108843512 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
32 00819917020625 108843511 108843511 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
33 00819917020618 108843510 108843510 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
34 00819917020601 108843509 108843509 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
35 00819917020595 108843508 108843508 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
36 00819917020588 108843507 108843507 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
37 00819917020571 108843506 108843506 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
38 00819917020564 108843505 108843505 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
39 00819917020557 108843312 108843312 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
40 00819917020540 108843311 108843311 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
41 00819917020533 108843310 108843310 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
42 00819917020526 108843309 108843309 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
43 00819917020519 108843308 108843308 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
44 00819917020502 108843307 108843307 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
45 00819917020496 108843306 108843306 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
46 00819917020489 108843305 108843305 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
47 00819917020472 108843012 108843012 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
48 00819917020465 108843011 108843011 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
49 00819917020458 108843010 108843010 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
50 00819917020441 108843009 108843009 ODP Intervertebral fusion device with bone graft, cervical 2 ACIS® ProTi 360°™
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