Other products from "EIT EMERGING IMPLANT TECHNOLOGIES GMBH"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 04260557775585 TFT30100 Implant Inserter MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT TLIF Inserter
2 04260557770313 CUI4080S CUI4080S ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 EIT CIF cage
3 04260614036567 LEC00101 LLIF instrument tray FSM Tray, Surgical, Instrument 1 EIT LLIF Instrument Tray
4 04260557839898 LEC00100 LLIF instrument tray OJH Orthopedic Tray 1 EIT LLIF Tray
5 04260557837733 LET30100 Implant Inserter MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT LLIF Inserter
6 04260557837702 LET20100 Trial Inserter MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT LLIF Inserter
7 04260397088227 PEC00101 PLIF Instrument Tray large FSM Tray, Surgical, Instrument 1 EIT PLIF Instrument Tray
8 04260397084120 PET91110 Trial, H: 11 mm, 18°, 30/9 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT PLIFTrial
9 04260397080870 PEC00100 PLIF Instrument Tray FSM Tray, Surgical, Instrument 1 EIT PLIF Instrument Tray
10 04260557836736 LET01160 Trial, H 11mm, 0°, 60/22 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT LLIF Trial
11 04260557836378 LET01140 Trial, H 11mm, 0°, 40/22 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT LLIF Trial
12 04260557833940 LUI01154 EIT LLIF, H 11mm, 0°, 55/18 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIZ LLIF cage
13 04260557774816 AET30121 Trial and Implant Guide, large MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Implant Guide
14 04260557774809 AET30120 Trial and Implant Guide, small MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Implant Guide
15 04260557774793 AET30110 Implant inserter knob SH Connection LXH Orthopedic Manual Surgical Instrument 1 EIT ALIF Inserter
16 04260557774670 AET71945 Trial, H 19mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
17 04260557774663 AET71845 Trial, H 18mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
18 04260557774656 AET71745 Trial, H 17mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
19 04260557774649 AET71645 Trial, H 16mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
20 04260557774632 AET71545 Trial, H 15mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
21 04260557774625 AET71445 Trial, H 14mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
22 04260557774618 AET71345 Trial, H 13mm, 20°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
23 04260557774595 AET51945 Trial, H 19mm, 15°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
24 04260557774588 AET51845 Trial, H 18mm, 15°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
25 04260557774557 AET51545 Trial, H 15mm, 15°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
26 04260557774540 AET51445 Trial, H 14mm, 15°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
27 04260557774533 AET51345 Trial, H 13mm, 15°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
28 04260557774496 AET31945 Trial, H 19mm, 10°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
29 04260557774465 AET31645 Trial, H 16mm, 10°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
30 04260557774441 AET31445 Trial, H 14mm, 10°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
31 04260557774168 AET01045 Trial, H 10mm, 0°, XL MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
32 04260557774120 AET71940 Trial, H 19mm, 20°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
33 04260557774113 AET71840 Trial, H 18mm, 20°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
34 04260557774106 AET71740 Trial, H 17mm, 20°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
35 04260557774069 AET71340 Trial, H 13mm, 20°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
36 04260557774052 AET71240 Trial, H 12mm, 20°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
37 04260557774038 AET51940 Trial, H 19mm, 15°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
38 04260557774021 AET51740 Trial, H 17mm, 15°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
39 04260557774007 AET51340 Trial, H 13mm, 15°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
40 04260557773994 AET51140 Trial, H 11mm, 15°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
41 04260557773970 AET31940 Trial, H 19mm, 10°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
42 04260397089989 AET01040 Trial, H 10mm, 0°, L MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
43 04260397089941 AET71937 Trial, H 19mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
44 04260397089934 AET71837 Trial, H 18mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
45 04260397089927 AET71737 Trial, H 17mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
46 04260397089903 AET71537 Trial, H 15mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
47 04260397089880 AET71337 Trial, H 13mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
48 04260397089873 AET71237 Trial, H 12mm, 20°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
49 04260397089835 AET51737 Trial, H 17mm, 15°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
50 04260397089828 AET51537 Trial, H 15mm, 15°, M MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 EIT ALIF Trial
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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