| 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 |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00841536119503 | 51234 | Suction w/Sals Tip Stylet | Thompson | THOMPSON SURGICAL INSTRUMENTS, INC. | |
| 2 | 00841536119466 | 51229 | Sals Tip Stylet | Thompson | THOMPSON SURGICAL INSTRUMENTS, INC. | |
| 3 | 00841523160488 | Tesera-k ALIF | 2167-013-001 | Angled Cover Plate Inserter | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 4 | 00841523160471 | Tesera-k ALIF | 2167-011-003 | Angled Tesera-k ALIF Cage Inserter | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 5 | 00841523158393 | Tesera-k ALIF | 2167-012-015 | Angled Retaining Hex Driver | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 6 | 00841523158355 | Tesera-k ALIF | 3167-006-000 | 27x24 Tesera-k A ALIF Instrument Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 7 | 00841523158348 | Tesera-k ALIF | 2168-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 8 | 00841523158331 | Tesera-k ALIF | 2168-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 9 | 00841523158324 | Tesera-k ALIF | 2168-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 10 | 00841523158317 | Tesera-k ALIF | 2168-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 11 | 00841523158300 | Tesera-k ALIF | 2168-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 12 | 00841523158294 | Tesera-k ALIF | 2168-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 13 | 00841523158287 | Tesera-k ALIF | 2168-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 14 | 00841523158270 | Tesera-k ALIF | 2168-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 15 | 00841523158263 | Tesera-k ALIF | 2168-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 16 | 00841523158256 | Tesera-k ALIF | 2168-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 17 | 00841523158249 | Tesera-k ALIF | 2167-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 18 | 00841523158232 | Tesera-k ALIF | 2167-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 19 | 00841523158225 | Tesera-k ALIF | 2167-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 20 | 00841523158218 | Tesera-k ALIF | 2167-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 21 | 00841523158201 | Tesera-k ALIF | 2167-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 22 | 00841523158195 | Tesera-k ALIF | 2167-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 23 | 00841523158188 | Tesera-k ALIF | 2167-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 24 | 00841523158171 | Tesera-k ALIF | 2167-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 25 | 00841523158164 | Tesera-k ALIF | 2167-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 26 | 00841523158157 | Tesera-k ALIF | 2167-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 27 | 00841523158140 | Tesera-k ALIF | 2167-134-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 12° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 28 | 00841523158133 | Tesera-k ALIF | 2167-131-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 12° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 29 | 00841523158126 | Tesera-k ALIF | 2167-042-209 | Tesera-k ALIF, 42W X 32D, 9.5mm, 7° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 30 | 00841523158119 | Tesera-k ALIF | 2167-038-009 | Tesera-k ALIF, 38W X 30D, 9.5mm, 7° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 31 | 00841523158102 | Tesera-k ALIF | 2167-034-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 7° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 32 | 00841523158096 | Tesera-k ALIF | 2167-031-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 7° Trial | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 33 | 00841523158072 | Tesera-k ALIF | 2167-000-000 | 27W x 24D Paddle Sizer | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 34 | 00841523158065 | Tesera-k ALIF | 2167-001-008 | Tesera-k A ALIF 27W x 24D Oblique Cage Inserter Tip | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 35 | 00841523158058 | Tesera-k ALIF | 2167-001-007 | Tesera-k A ALIF Oblique Cage Inserter Tip | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 36 | 00841523158041 | Tesera-k ALIF | 2167-001-006 | Tesera-k A ALIF Cage Inserter Tip | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 37 | 00841523157877 | Tesera-k ALIF | 3167-005-000 | Tesera-k ALIF Broach Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 38 | 00841523157860 | Tesera-k ALIF | 3167-004-000 | Tesera-k ALIF Trial Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 39 | 00841523157853 | Tesera-k ALIF | 3167-003-001 | Tesera-k ALIF Screw and Coverplate Insertion Case Inner Tray 1 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 40 | 00841523157846 | Tesera-k ALIF | 3167-003-000 | Tesera-k ALIF Screw and Coverplate Insertion Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 41 | 00841523157839 | Tesera-k ALIF | 3167-002-001 | Tesera-k ALIF Cage Insertion Case Inner Tray 1 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 42 | 00841523157822 | Tesera-k ALIF | 3167-002-000 | Tesera-k ALIF Cage Insertion Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 43 | 00841523157815 | Tesera-k ALIF | 3167-001-002 | Tesera-k ALIF Disc Prep Case Inner Tray 2 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 44 | 00841523157808 | Tesera-k ALIF | 3167-001-001 | Tesera-k ALIF Disc Prep Case Inner Tray 1 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 45 | 00841523157792 | Tesera-k ALIF | 3167-001-000 | Tesera-k ALIF Disc Prep Case | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 46 | 00841523157778 | Tesera-k ALIF | 2168-342-221 | Tesera-k ALIF, 42W X 32D, 21mm, 22° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 47 | 00841523157761 | Tesera-k ALIF | 2168-342-219 | Tesera-k ALIF, 42W X 32D, 19mm, 22° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 48 | 00841523157754 | Tesera-k ALIF | 2168-342-217 | Tesera-k ALIF, 42W X 32D, 17mm, 22° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 49 | 00841523157747 | Tesera-k ALIF | 2168-338-021 | Tesera-k ALIF, 38W X 30D, 21mm, 22° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |
| 50 | 00841523157730 | Tesera-k ALIF | 2168-338-019 | Tesera-k ALIF, 38W X 30D, 19mm, 22° Broach | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. |