Other products from "GLOBUS MEDICAL, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00849044083866 652.632 Single Trial, 32mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
2 00849044083859 652.630 Single Trial, 30mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
3 00849044092882 688.400 Rod Cutter LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
4 00849044076011 601.405 Trial, Parallel, 5mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
5 00849044072389 685.420 Calipers LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
6 00849044056075 624.613 REVERE Power Bender LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
7 00849044092875 688.368 Small Plate Caddy LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
8 00849044092868 688.367 AP Inserter Caddy LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
9 00849044092851 688.366 AP Inserter, 44-55mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
10 00849044092844 688.365 AP Inserter, 35-41mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
11 00849044092905 688.460 SP-Fix ARC Plate Pincher LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
12 00849044092899 688.450 Plate Pincher LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
13 00849044086089 671.303 Screwdriver Sleeve LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
14 00849044092837 688.351 Lateral Barrel Inserter, 44-55mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
15 00849044092820 688.350 Lateral Barrel Inserter, 35-41mm Plate LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
16 00849044092813 688.331 Removal Driver LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
17 00849044092806 688.330 Hex Key LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
18 00849044092790 688.320 Implant Compressor LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
19 00849044092783 688.315 Rod Holder LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
20 00849044092776 688.314 Barrel Holder LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
21 00849044092769 688.311 Plate Holder, 44-55mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
22 00849044092752 688.310 Plate Holder, 35-41mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
23 00849044092745 688.300 Distractor LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
24 00849044092738 688.275 Rod Trial LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
25 00849044092721 688.255 Plate Trial, 55mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
26 00849044092714 688.250 Plate Trial, 50mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
27 00849044092707 688.247 Plate Trial, 47mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
28 00849044092691 688.244 Plate Trial, 44mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
29 00849044092684 688.241 Plate Trial, 41mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
30 00849044092677 688.238 Plate Trial, 38mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
31 00849044092660 688.235 Plate Trial, 35mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
32 00849044092653 688.232 Plate Trial, 32mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
33 00849044092646 688.229 Plate Trial, 29mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
34 00849044092615 688.170 LP-Ti Barrel Trial, 20mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
35 00849044092608 688.168 LP-Ti Barrel Trial, 18mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
36 00849044092592 688.166 LP-Ti Barrel Trial, 16mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
37 00849044092585 688.164 LP-Ti Barrel Trial, 14mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
38 00849044092578 688.162 LP-Ti Barrel Trial, 12mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
39 00849044092561 688.160 LP-Ti Barrel Trial, 10mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
40 00849044092554 688.158 LP-Ti Barrel Trial, 8mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
41 00849044092530 688.120 Trial, 20mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
42 00849044092523 688.118 Trial, 18mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
43 00849044092516 688.116 Trial, 16mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
44 00849044092509 688.114 Trial, 14mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
45 00849044092493 688.112 Trial, 12mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
46 00849044092486 688.110 Trial, 10mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
47 00849044092479 688.108 Trial, 8mm LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
48 00849044092462 688.075 Rasp LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
49 00849044092455 688.060 Spinous Process Rake LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
50 00849044089837 524.885 8.5mm REVERE Monoaxial Reduction Screw, 90mm KWP,MNH,KWQ,NKB,MNI APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixa APPLIANCE, FIXATION, SPINAL INTERLAMINAL,Orthosis, spondylolisthesis spinal fixation,APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY,Orthosis, spinal pedicle fixation, for degenerative disc disease,ORTHOSIS, SPINAL PEDICLE FIXATION 2 REVERE
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.
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