Other products from "HT MEDICAL, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00818345024748 23-LCN-3006 N/A Ti3D CAGE, 10W x 30L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
2 00818345024731 23-LCN-2806 N/A Ti3D CAGE, 10W x 28L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
3 00818345024724 23-LCN-2506 N/A Ti3D CAGE, 10W x 25L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
4 00818345024717 23-LCN-2206 N/A Ti3D CAGE, 10W x 22L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
5 00818345024700 23-LCN-2006 N/A Ti3D CAGE, 10W x 20L x 6H, 0 DEG, STRAIGHT MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TIWAVE L
6 00818345027251 B04-02 Universal Handle, Cervical, Double Sided LXH Orthopedic Manual Surgical Instrument 1 Ti3D CERVICAL
7 00818345026773 C1412-04 Ti3D CAGE 14W x 12D x 4H, 6 DEG ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 NeoFuse Ti3D CERVICAL
8 00818345026261 20-RAT-9405 N/A CERVICAL RASP, 19 X 14 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
9 00818345026254 20-RAT-7305 N/A CERVICAL RASP, 17 X 13 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
10 00818345026247 20-RAT-5205 N/A CERVICAL RASP, 15 X 12 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
11 00818345026230 20-RAT-3205 N/A CERVICAL RASP, 13 X 12 X 5MM, 7°, ANATOMIC LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
12 00818345026223 20-RFT-9405 N/A CERVICAL RASP, 19 X 14 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
13 00818345026216 20-RFT-7305 N/A CERVICAL RASP, 17 X 13 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
14 00818345026209 20-RFT-5205 N/A CERVICAL RASP, 15 X 12 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
15 00818345026193 20-RFT-3205 N/A CERVICAL RASP, 13 X 12 X 5MM, 7°, FLAT LXH Orthopedic Manual Surgical Instrument 1 TIWAVE
16 00818345026186 20-CFT-9412 N/A TI3D CAGE, 19W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
17 00818345026179 20-CFT-9411 N/A TI3D CAGE, 19W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
18 00818345026162 20-CFT-9410 N/A TI3D CAGE, 19W X 12D X 10H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
19 00818345026155 20-CFT-9409 N/A TI3D CAGE, 19W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
20 00818345026148 20-CFT-9408 N/A TI3D CAGE, 19W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
21 00818345026131 20-CFT-9407 N/A TI3D CAGE, 19W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
22 00818345026124 20-CFT-9406 N/A TI3D CAGE, 19W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
23 00818345026117 20-CFT-9405 N/A TI3D CAGE, 19W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
24 00818345026032 C1211-04 Ti3D CAGE 12W x 11.5D x 4H, 6 DEG ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 NeoFuse Ti3D CERVICAL
25 00818345026025 20-CFX-5212 N/A Ti3D Cage, 15W x 12D x 12H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
26 00818345026018 20-CFX-5211 N/A Ti3D Cage, 15W x 12D x 11H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
27 00818345026001 20-CFX-5210 N/A Ti3D Cage, 15W x 12D x 10H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
28 00818345025998 20-CFX-5209 N/A Ti3D Cage, 15W x 12D x 9H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
29 00818345025981 20-CFX-5208 N/A Ti3D Cage, 15W x 12D x 8H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
30 00818345025974 20-CFX-5207 N/A Ti3D Cage, 15W x 12D x 7H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
31 00818345025967 20-CFX-5206 N/A Ti3D Cage, 15W x 12D x 6H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
32 00818345025950 20-CFX-5205 N/A Ti3D Cage, 15W x 12D x 5H, 14 Deg, Flat ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
33 00818345025943 20-CFT-7312 N/A TI3D CAGE, 17W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
34 00818345025936 20-CFT-7311 N/A TI3D CAGE, 17W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
35 00818345025929 20-CFT-7310 N/A TI3D CAGE, 17W X 12D X 10H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
36 00818345025912 20-CFT-7309 N/A TI3D CAGE, 17W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
37 00818345025905 20-CFT-7308 N/A TI3D CAGE, 17W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
38 00818345025899 20-CFT-7307 N/A TI3D CAGE, 17W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
39 00818345025882 20-CFT-7306 N/A TI3D CAGE, 17W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
40 00818345025875 20-CFT-7305 N/A TI3D CAGE, 17W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
41 00818345025868 20-CFT-5212 N/A TI3D CAGE, 15W X 12D X 12H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
42 00818345025851 20-CFT-5211 N/A TI3D CAGE, 15W X 12D X 11H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
43 00818345025844 20-CFT-5210 N/A TI3D CAGE, 15W X 12D X 10H, 7DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
44 00818345025837 20-CFT-5209 N/A TI3D CAGE, 15W X 12D X 9H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
45 00818345025820 20-CFT-5208 N/A TI3D CAGE, 15W X 12D X 8H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
46 00818345025813 20-CFT-5207 N/A TI3D CAGE, 15W X 12D X 7H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
47 00818345025806 20-CFT-5206 N/A TI3D CAGE, 15W X 12D X 6H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
48 00818345025790 20-CFT-5205 N/A TI3D CAGE, 15W X 12D X 5H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
49 00818345025783 20-CFT-3212 N/A TI3D CAGE, 13W X 12D X 12H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
50 00818345025776 20-CFT-3211 N/A TI3D CAGE, 13W X 12D X 11H, 7 DEG, FLAT ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 TIWAVE
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.
17 00812998044399 CSTS-000022 CSTS-000022 4WEB Medical 4WEB MEDICAL
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