Other products from "ZIMMER SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024331891 1875-314 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
2 00889024331884 1875-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
3 00889024331877 1875-310 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
4 00889024331860 1875-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
5 00889024331853 1875-114 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
6 00889024331846 1875-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
7 00889024331839 1875-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
8 00889024331822 1875-108 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
9 00889024331815 1874-500 1874-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
10 00889024331808 1874-300 1874-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
11 00889024331792 1874-100 1874-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
12 00889024331785 1873-1 1873-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
13 00889024331778 1872-2 1872-2 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
14 00889024332041 1894-400 1894-400 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
15 00889024331761 1871-1 1871-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
16 00889024331754 1870-1 1870-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
17 00889024331747 1869-1 1869-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
18 00889024331730 1868-14 1868-14 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
19 00889024331723 1868-12 1868-12 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
20 00889024331716 1868-10 1868-10 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
21 00889024331709 1868-08 1868-08 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
22 00889024331693 1865-514 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
23 00889024331686 1865-512 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
24 00889024332058 1894-500 1894-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
25 00889024332034 1894-300 1894-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
26 00889024332027 1894-200 1894-200 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
27 00889024332010 1894-100 1894-100 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
28 00889024332003 1879-500 1879-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
29 00889024331990 1879-300 1879-300 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
30 00889024331983 1879-100 1879-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
31 00889024331976 1877-500 1877-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
32 00889024331969 1877-300 1877-300 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
33 00889024331952 1877-100 1877-100 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
34 00889024331945 1876-1 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
35 00889024331938 1875-514 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
36 00889024331921 1875-512 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
37 00889024331914 1875-510 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
38 00889024331907 1875-508 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
39 00889024331679 1865-510 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
40 00889024331662 1865-508 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
41 00889024331655 1865-314 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
42 00889024331648 1865-312 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
43 00889024331631 1865-310 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
44 00889024331624 1865-308 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
45 00889024331617 1865-114 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
46 00889024331600 1865-112 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
47 00889024331594 1865-110 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
48 00889024331587 1865-108 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
49 00889024331563 1859-1 1859-1 MQP,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 2 InFix®
50 00889024331556 1857-500 1857-500 MAX,MQP Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE 2 InFix®
Other products with the same Product Codes "KWP, MNH, MNI"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00813892021073 CN3010 CN3010 Cross Link Nut Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
2 00813892021066 CH2010 CH2010 Cross Link Hook Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
3 00813892021059 TL1080 TL1080 80mm Cross Link Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
4 00813892021042 TL1070 TL1070 70mm Cross Link Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
5 00813892021035 TL1060 TL1060 60mm Cross Link Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
6 00813892021028 TL1050 TL1050 50mm Cross Link Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
7 00813892021011 TL1040 TL1040 40mm Cross Link Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
8 00813892021004 SS6020 SS6020 Set Screw Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
9 00813892020991 RD6150 RD6150 6.0 x 150mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
10 00813892020984 RD6120 RD6120 6. 0x 120mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
11 00813892020977 RD6100 RD6100 6.0 x 100mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
12 00813892020960 RD6090 RD6090 6.0 x 90mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
13 00813892020953 RD6080 RD6080 6.0 x 80mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
14 00813892020946 RD6070 RD6070 6.0 x 70mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
15 00813892020939 RD6060 RD6060 6.0 x 60mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
16 00813892020922 RD6050 RD6050 6.0 x 50mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
17 00813892020915 RD6040 RD6040 6.0 x 40mm Titanium Rod Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
18 00813892020908 PS7060 PS7060 7.0 X 60mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
19 00813892020892 PS7055 PS7055 7.0 X 55mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
20 00813892020885 PS7050 PS7050 7.0 X 50mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
21 00813892020878 PS7045 PS7045 7.0 X 45mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
22 00813892020861 PS7040 PS7040 7.0 X 40mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
23 00813892020854 PS7035 PS7035 7.0 X 35mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
24 00813892020847 PS7030 PS7030 7.0 X 30mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
25 00813892020830 PS6060 PS6060 6.0 X 60mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
26 00813892020823 PS6055 PS6055 6.0 X 55mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
27 00813892020816 PS6050 PS6050 6.0 X 50mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
28 00813892020809 PS6045 PS6045 6.0 X 45mmTitanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
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31 00813892020779 PS6030 PS6030 6.0 X 30mm Titanium Pedicle Screw Self Tapping Outologous Spinal Fixation System ORTHOPEDIC SCIENCES INC
32 00813210022300 800-0235 Polyaxial Plate Inserter primaLOK SP WENZEL SPINE, INC.
33 00813210022294 800-0233 Post Plate Inserter primaLOK SP WENZEL SPINE, INC.
34 00813210022287 800-0228 Offset Provisional Locker primaLOK SP WENZEL SPINE, INC.
35 00813210022270 800-0227 Inserter Compressor II primaLOK SP WENZEL SPINE, INC.
36 00813210022263 800-0203 Removal Tool primaLOK SP WENZEL SPINE, INC.
37 00813210022256 800-0201 Lock Ring Compressor primaLOK SP WENZEL SPINE, INC.
38 00813210022249 800-0200 Implant Inserter primaLOK SP WENZEL SPINE, INC.
39 00813210021785 800-0828-00 primaLOK SP 28mm Medium Boxless Implant, Sterile primaLOK SP 28mm Medium Boxless Implant, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
40 00813210021778 800-0118-00 primaLOK SP 18mm Implant Assembly, Sterile primaLOK SP 18mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
41 00813210021761 800-0115-00 primaLOK SP 15mm Implant Assembly, Sterile primaLOK SP 15mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
42 00813210021754 800-0112-00 primaLOK SP 12mm Implant Assembly, Sterile primaLOK SP 12mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
43 00813210021747 800-0110-00 primaLOK SP 10mm Implant Assembly, Sterile primaLOK SP 10mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
44 00813210021730 800-0108-00 primaLOK SP 8mm Implant Assembly, Sterile primaLOK SP 8mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
45 00813210021723 800-0106-00 primaLOK SP 6mm Implant Assembly, Sterile primaLOK SP 6mm Implant Assembly, Sterile The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use. primaLOK SP WENZEL SPINE, INC.
46 00813210021365 800-0501 Auxiliary Instrument Case primaLOK SP WENZEL SPINE, INC.
47 00813210021358 800-0500 Instrument Case primaLOK SP WENZEL SPINE, INC.
48 00812352021318 4302081 Royal Oak Pedicle Screw Instrument Set Case 2 Royal Oak Pedicle Screw System ROYAL OAK MEDICAL DEVICES LLC
49 00812352021318 4302081 Royal Oak Pedicle Screw Instrument Set Case 2 Royal Oak Pedicle Screw System ROYAL OAK MEDICAL DEVICES LLC
50 00812352021301 4301081 Royal Oak Pedicle Screw Instrument Set Case 1 Royal Oak Pedicle Screw System ROYAL OAK MEDICAL DEVICES LLC