Other products from "WENZEL SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00813210022300 800-0235 Polyaxial Plate Inserter KWP Appliance, Fixation, Spinal Interlaminal 2 primaLOK SP
2 00813210022294 800-0233 Post Plate Inserter KWP Appliance, Fixation, Spinal Interlaminal 2 primaLOK SP
3 00813210022096 800-1206 EMG Cannula LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
4 00813210022157 800-1221 3mm Cannulated Power Drill LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
5 00813210022133 800-1215 Ratcheting Driver Handle LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
6 00813210022126 800-1210 Cannula Inserter LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
7 00813210022119 800-1208 Single Bevel Access Needle (sterile, single use) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
8 00813210022102 800-1207 Access Needle (sterile, single use) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
9 00813210022089 800-1205 Standard Cannula LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
10 00813210022072 800-1204 Guide Wire Stiffener LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
11 00813210022065 800-1202 Cannulated Tap LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
12 00813210022041 800-1200 Guide Wire (single use, disposable) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
13 00813210022034 800-1213 Threaded Implant Holder Shaft - Solid MRW System, Facet Screw Spinal Device U primaLOK FF
14 00813210022027 800-1212 Threaded Implant Holder Shaft - Cannulated MRW System, Facet Screw Spinal Device U primaLOK FF
15 00813210022010 800-1211 Implant Driver MRW System, Facet Screw Spinal Device U primaLOK FF
16 00813210022003 800-1203 Removal Driver MRW System, Facet Screw Spinal Device U primaLOK FF
17 00813210021990 800-1145-00 primaLOK FF 45mm Implant Assembly, Sterile primaLOK FF 45mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
18 00813210021983 800-1140-00 primaLOK FF 40mm Implant Assembly, Sterile primaLOK FF 40mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
19 00813210021976 800-1135-00 primaLOK FF 35mm Implant Assembly, Sterile primaLOK FF 35mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
20 00813210021969 800-1130-00 primaLOK FF 30mm Implant Assembly, Sterile primaLOK FF 30mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
21 00813210021952 800-1125-00 primaLOK FF 25mm Implant Assembly, Sterile primaLOK FF 25mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
22 00813210021945 800-1501 Percutaneous Instrument Case LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
23 00813210021938 800-1500 Instrument Case LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
24 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
25 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
26 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
27 00813210020825 CIC2-A750 VariLift-C Unlocking Rod LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
28 00813210020818 CIC2-A746 VariLift-C 10mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
29 00813210020801 CIC2-A745 VariLift-C 09mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
30 00813210020795 CIC2-A744 VariLift-C 08mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
31 00813210020788 CIC2-A743 Expander ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
32 00813210020771 CIC2-A742 Retainer ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
33 00813210020764 CIC2-A741 Inserter ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
34 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
35 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
36 00813210020269 CIC1-A749 Graft Ejector LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
37 00813210020252 CIC1-A747 Removal Screwdriver ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
38 00813210020245 CIC1-A745 Tap, 9.0mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
39 00813210020238 CIC1-A744 Tap, 7.5mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
40 00813210020221 CIC1-A743 Expansion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
41 00813210020214 CIC1-A742 Locking Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
42 00813210020207 CIC1-A741 Insertion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
43 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
44 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
45 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
46 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
47 00813210021341 CIC2-A001 VariLift-C Instrument Case LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
48 00813210022393 800-0306 Implant Sizer - 6mm LXH Orthopedic Manual Surgical Instrument 1 primaLOK-SP
49 00813210020696 CIE3-A128 Expander, 28mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 VariLift-LX
50 00813210020689 CIE3-A124 Expander, 24mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 VariLift-LX
Other products with the same Product Code "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M695502P267812S1 502-P267812-S 502-P267812-S PLIF 26mm x 12mm x 7mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
2 M695502P267810S1 502-P267810-S 502-P267810-S PLIF 26mm x 10mm x 7mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
3 M695502P26748S1 502-P26748-S 502-P26748-S PLIF 26mm x 8mm x 7mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
4 M695502P267412S1 502-P267412-S 502-P267412-S PLIF 26mm x 12mm x 7mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
5 M695502P267410S1 502-P267410-S 502-P267410-S PLIF 26mm x 10mm x 7mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
6 M695502P2670S0 PLIF 26mm x 8mm x 7mm x 0 Degree 502-P26708-S Tyber Medical TYBER MEDICAL LLC
7 M695502P26708S1 502P26708-S 502P26708-S PLIF 26mm x 8mm x 7mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
8 M695502P267012S1 502-P267012-S 502-P267012-S PLIF 26mm x 12mm x 7mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
9 M695502P267012S0 PLIF 26mm x 12mm x 7mm x 0 degree 502-P267012-S Tyber Medical TYBER MEDICAL LLC
10 M695502P267010S1 502-P267010-S 502-P267010-S PLIF 26mm x 10mm x 7mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
11 M695502P267010S0 PLIF 26mm x 10mm x 7mm x 0 Degree 502-P267010-S Tyber Medical TYBER MEDICAL LLC
12 M695502P261788S1 502-P261788-S 502-P261788-S PLIF 26mm x 8mm x 17mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
13 M695502P2617812S1 502-P2617812-S 502-P2617812-S PLIF 26mm x 12mm x 17mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
14 M695502P2617810S1 502-P2617810-S 502-P2617810-S PLIF 26mm x 10mm x 17mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
15 M695502P261748S1 502-P261748-S 502-P261748-S PLIF 26mm x 8mm x 17mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
16 M695502P2617412S1 502-P2617412-S 502-P2617412-S PLIF 26mm x 12mm x 17mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
17 M695502P2617410S1 502-P2617410-S 502-P2617410-S PLIF 26mm x 10mm x 17mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
18 M695502P261708S1 502-P261708-S 502-P261708-S PLIF 26mm x 8mm x 17mm x 0 °,TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
19 M695502P261708S0 PLIF 26mm x 8mm x 17mm x 0 Degree 502-P261708-S Tyber Medical TYBER MEDICAL LLC
20 M695502P2617012S1 502-P2617012-S 502-P2617012-S PLIF 26mm x 12mm x 17mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
21 M695502P2617012S0 PLIF 26mm x 12mm x 17mm x 0 degree 502-P2617012-S Tyber Medical TYBER MEDICAL LLC
22 M695502P2617010S1 502-P2617010-S 502-P2617010-S PLIF 26mm x 10mm x 17mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
23 M695502P2617010S0 PLIF 26mm x 10mm x 17mm x 0 Degree 502-P2617010-S Tyber Medical TYBER MEDICAL LLC
24 M695502P261688S1 502-P261688-S 502-P261688-S PLIF 26mm x 8mm x 16mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
25 M695502P2616812S1 502-P2616812-S 502-P2616812-S PLIF 26mm x 12mm x 16mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
26 M695502P2616810S1 502-P2616810-S 502-P2616810-S PLIF 26mm x 10mm x 16mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
27 M695502P261648S1 502-P261648-S 502-P261648-S PLIF 26mm x 8mm x 16mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
28 M695502P2616412S1 502-P2616412-S 502-P2616412-S PLIF 26mm x 12mm x 16mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
29 M695502P2616410S1 502-P2616410-S 502-P2616410-S PLIF 26mm x 10mm x 16mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
30 M695502P261608S1 502-P261608-S 502-P261608-S PLIF 26mm x 8mm x 16mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
31 M695502P261608S0 PLIF 26mm x 8mm x 16mm x 0 Degree 502-P261608-S Tyber Medical TYBER MEDICAL LLC
32 M695502P2616012S1 502-P2616012-S 502-P2616012-S PLIF 26mm x 12mm x 16mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
33 M695502P2616012S0 PLIF 26mm x 12mm x 16mm x 0 degree 502-P2616012-S Tyber Medical TYBER MEDICAL LLC
34 M695502P2616010S1 502-P2616010-S 502-P2616010-S PLIF 26mm x 10mm x 16mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
35 M695502P2616010S0 PLIF 26mm x 10mm x 16mm x 0 Degree 502-P2616010-S Tyber Medical TYBER MEDICAL LLC
36 M695502P261588S1 502-P261588-S 502-P261588-S PLIF 26mm x 8mm x 15mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
37 M695502P2615812S1 PLIF 26mm x 12mm x 15mm x 8 °, TyPEEK, Sterile 502-P2615812S-S Tyber Medical TYBER MEDICAL LLC
38 M695502P2615810S1 502-P2615810-S 502-P2615810-S PLIF 26mm x 10mm x 15mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
39 M695502P261548S1 502-P261548-S 502-P261548-S PLIF 26mm x 8mm x 15mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
40 M695502P2615412S1 502-P2615412-S 502-P2615412-S PLIF 26mm x 12mm x 15mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
41 M695502P2615410S1 502-P2615410-S 502-P2615410-S PLIF 26mm x 10mm x 15mm x 4 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
42 M695502P261508S1 502-P261508-S 502-P261508-S PLIF 26mm x 8mm x 15mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
43 M695502P261508S0 PLIF 26mm x 8mm x 15mm x 0 Degree 502-P261508-S Tyber Medical TYBER MEDICAL LLC
44 M695502P2615012S1 502-P2615012-S 502-P2615012-S PLIF 26mm x 12mm x 15mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
45 M695502P2615012S0 PLIF 26mm x 12mm x 15mm x 0 degree 502-P2615012-S Tyber Medical TYBER MEDICAL LLC
46 M695502P2615010S1 502-P2615010-S 502-P2615010-S PLIF 26mm x 10mm x 15mm x 0 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
47 M695502P2615010S0 PLIF 26mm x 10mm x 15mm x 0 Degree 502-P2615010-S Tyber Medical TYBER MEDICAL LLC
48 M695502P261488S1 502-P261488-S 502-P261488-S PLIF 26mm x 8mm x 14mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
49 M695502P2614812S1 502-P2614812-S 502-P2614812-S PLIF 26mm x 12mm x 14mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC
50 M695502P2614810S1 502-P2614810-S 502-P2614810-S PLIF 26mm x 10mm x 14mm x 8 °, TyPEEK, Sterile Tyber Medical TYBER MEDICAL LLC