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 "LXH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 37613154881872 6003-003-090 6003-003-090 PINABALL PRELOADED PINS PINABALL STRYKER LEIBINGER GMBH & CO. KG
2 37613154571421 01-04175 01-04175 US ARMY RETRACTORS NA STRYKER LEIBINGER GMBH & CO. KG
3 37613154126713 52-00040 52-00040 Screw Length Marker for 40mm NA STRYKER TRAUMA SA
4 37613154126706 52-00035 52-00035 Screw Length Marker for 35mm NA STRYKER TRAUMA SA
5 30845854902329 KBR191 KBR191 Infinity Anteromedial Guide Right 9/10mm Infinity CONMED CORPORATION
6 30845854902312 KBR178 KBR178 Infinity Anteromedial Guide Right 7/8mm Infinity CONMED CORPORATION
7 30845854902305 KBL191 KBL191 Infinity Anteromedial Guide Left 9/10mm Infinity CONMED CORPORATION
8 30845854902299 KBL178 KBL178 Infinity Anteromedial Guide Left 7/8mm Infinity CONMED CORPORATION
9 30845854902282 KGB100 KGB100 Infinity Guide Body Infinity CONMED CORPORATION
10 30845854902275 KTS135 KTS135 Infinity 3.5mm All-Inside Guide Sleeve Infinity CONMED CORPORATION
11 30845854902268 KTS224 KTS224 Infinity 2.4mm Guide Sleeve Angled Infinity CONMED CORPORATION
12 30845854902251 KTS124 KTS124 Infinity 2.4mm Guide Sleeve Straight Infinity CONMED CORPORATION
13 30845854902244 KTP100 KTP100 Infinity PCL Tibial Guide Infinity CONMED CORPORATION
14 30845854902237 KTT100 KTT100 Infinity ACL Tibial Tip Guide Infinity CONMED CORPORATION
15 30845854902220 KTE100 KTE100 Infinity ACL Tibial Elbow Guide Infinity CONMED CORPORATION
16 30845854902213 KTA100 KTA100 Infinity ACL Tibial Footprint Guide Infinity CONMED CORPORATION
17 30845854902206 KFA100 KFA100 Infinity ACL/PCL Femoral Footprint Guide Infinity CONMED CORPORATION
18 30845854902190 KFD035 KFD035 Infinity 3.5mm Tunnel Dilator Infinity CONMED CORPORATION
19 30845854648852 KTT100 KTT100 Infinity ACL Tibial Tip Guide Infinity CONMED CORPORATION
20 30845854648814 KTP100 KTP100 Infinity PCL Tibial Guide Infinity CONMED CORPORATION
21 30845854648807 KTE100 KTE100 Infinity ACL Tibial Elbow Guide Infinity CONMED CORPORATION
22 30845854648791 KTA100 KTA100 Infinity ACL Tibial Footprint Guide Infinity CONMED CORPORATION
23 30845854648784 KGB100 KGB100 Infinity Guide Body Infinity CONMED CORPORATION
24 30845854648777 KFA100 KFA100 Infinity ACL/PCL Femoral Footprint Guide Infinity CONMED CORPORATION
25 30845854648760 KBR191 KBR191 Infinity Anteromedial Guide Right 9/10mm Infinity CONMED CORPORATION
26 30845854648753 KBR178 KBR178 Infinity Anteromedial Guide Right 7/8mm Infinity CONMED CORPORATION
27 30845854648746 KBL191 KBL191 Infinity Anteromedial Guide Left 9/10mm Infinity CONMED CORPORATION
28 30845854648739 KBL178 KBL178 Infinity Anteromedial Guide Left 7/8mm Infinity CONMED CORPORATION
29 30845854648616 PGU701 PGU701 Paradigm Slim Suture Retriever, 15 Degree Up Paradigm CONMED CORPORATION
30 30845854648609 PGU700 PGU700 Paradigm Slim Raven Suture Passer, 15 deg Up Paradigm CONMED CORPORATION
31 30845854083639 KFD035 KFD035 Infinity 3.5mm Tunnel Dilator Infinity CONMED CORPORATION
32 30845854082328 PCKP PCKP Paradigmâ„¢Curved Knot Pusher PARADIGM CONMED CORPORATION
33 30845854052864 P9305 P9305 MERLIN MULTI-BENDING FIXTURE MERLIN CONMED CORPORATION
34 30845854034082 C8016 C8016 BIOSCREW GUIDE WIRES, 356MM (14 IN), QTY 5 BIOSCREW CONMED CORPORATION
35 30845854016675 C8026 C8026 BIOSCREW HYPERFLEX GUIDEWIRES, 356MM (14 IN.), QTY 5 BIOSCREW CONMED CORPORATION
36 30653405987141 2101-02-010 2101-02-010 ExoShape Sheath Inserter 10 mm ExoShape CONMED CORPORATION
37 30653405987042 2500-10-000 2500-10-000 ExoShape Removal Tool Femoral ExoShape CONMED CORPORATION
38 30653405987035 2101-06-000 2101-06-000 ExoShape Instrument Caddy ExoShape CONMED CORPORATION
39 30653405987028 2101-00-000 2101-00-000 ExoShape Gun Tibial ExoShape CONMED CORPORATION
40 30653405987011 2101-05-000 2101-05-000 ExoShape Removal Tool Tibial ExoShape CONMED CORPORATION
41 30653405987004 2101-03-000 2101-03-000 ExoShape Graft Bar ExoShape CONMED CORPORATION
42 30653405986991 2101-02-012 2101-02-012 ExoShape Sheath Inserter 12 mm ExoShape CONMED CORPORATION
43 30653405986984 2101-02-011 2101-02-011 ExoShape Sheath Inserter 11 mm ExoShape CONMED CORPORATION
44 30653405986977 2101-02-009 2101-02-009 ExoShape Sheath Inserter 9 mm ExoShape CONMED CORPORATION
45 30653405986960 2101-02-008 2101-02-008 ExoShape Sheath Inserter 8 mm ExoShape CONMED CORPORATION
46 30653405986953 2101-02-007 2101-02-007 ExoShape Sheath Inserter 7 mm ExoShape CONMED CORPORATION
47 30653405986946 2101-01-011 2101-01-011 ExoShape Trialator 11 mm ExoShape CONMED CORPORATION
48 30653405986939 2101-01-010 2101-01-010 ExoShape Trialator 10 mm ExoShape CONMED CORPORATION
49 30653405986922 2101-01-009 2101-01-009 ExoShape Trialator 9 mm ExoShape CONMED CORPORATION
50 30653405986915 2101-01-008 2101-01-008 ExoShape Trialator 8 mm ExoShape CONMED CORPORATION