No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00840996177641 | P070-32186W | TIGER SHARK STRAIGHT TRIAL 11x32X18-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
2 | 00840996177634 | P070-32186W | TIGER SHARK STRAIGHT TRIAL 11x32X18-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
3 | 00840996177627 | P070-32176W | TIGER SHARK STRAIGHT TRIAL 11x32X17-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
4 | 00840996177610 | P070-32166W | TIGER SHARK STRAIGHT TRIAL 11x32X16 6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
5 | 00840996177603 | P070-32156W | TIGER SHARK STRAIGHT TRIAL 11x32X15-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
6 | 00840996177597 | P070-32146W | TIGER SHARK STRAIGHT TRIAL 11x32X14-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
7 | 00840996177580 | P070-32136W | TIGER SHARK STRAIGHT TRIAL 11x32X13-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
8 | 00840996177573 | P070-32126W | TIGER SHARK STRAIGHT TRIAL 11x32X12-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
9 | 00840996177566 | P070-32116W | TIGER SHARK STRAIGHT TRIAL 11x32X11-6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
10 | 00840996177559 | P070-28176W | TIGER SHARK STRAIGHT TRIAL 11x28x17 6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
11 | 00840996177542 | P070-28166W | TIGER SHARK STRAIGHT TRIAL 11x28x16 6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
12 | 00840996177535 | P070-28156W | TIGER SHARK STRAIGHT TRIAL 11x28x15 6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
13 | 00840996177528 | P070-28146W | TIGER SHARK STRAIGHT TRIAL 11x28x14 6DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
14 | 00840996177511 | P070-28136W | TIGER SHARK STRAIGHT TRIAL 11x28x13 6deg | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
15 | 00840996177504 | P070-28126W | TIGER SHARK STRAIGHT TRIAL 11x28x12 6deg | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
16 | 00840996177498 | P070-28116W | TIGER SHARK STRAIGHT TRIAL 11x28x11-6deg | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
17 | 00840996177481 | P070-28106W | TIGER SHARK STRAIGHT TRIAL 11x28x10 6deg | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
18 | 00840996177474 | P070-24166W | TIGER SHARK,STRAIGHT,TRIAL,9X32X16-6 DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
19 | 00840996177467 | P070-24156W | TIGER SHARK,STRAIGHT,TRIAL,9X32X15-6 DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
20 | 00840996177450 | P070-24146W | TIGER SHARK,STRAIGHT,TRIAL,9X24X14,6 DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
21 | 00840996177443 | P070-24136W | TIGER SHARK,STRAIGHT,TRIAL,9X32X13,6 DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
22 | 00840996177436 | P070-24126W | TIGER SHARK,STRAIGHT,TRIAL,9X32X12,6 DEG | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
23 | 00840996177429 | P070-24116W | Tiger Shark Trial 11X24x11-6 deg | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tiger Shark Spinal System | |
24 | 00840996177412 | P070-24106W | Tiger Shark Trial 11X24x10-6 deg | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tiger Shark Spinal System | |
25 | 00840996177405 | P070-24096W | Tiger Shark Trial 11X24x9-6 deg | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tiger Shark Spinal System | |
26 | 00840996177276 | V070-1003R | Tiger Shark, Inserter,Angled, Right | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | Tiger Shark Spinal System | |
27 | 00840996157452 | SK-002606 | PROLIANT, SLEEVE, GLOVE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Proliant Polyaxial Pedicle Screw System | |
28 | 00840996157445 | BSK-9663 | PROLIANT, HEAD POSITIONER | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Proliant Polyaxial Pedicle Screw System | |
29 | 00840996157421 | 301-07-80 | HANDLE,UNIV,RATCHET,DRIVER,HUDSON | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Proliant Polyaxial Pedicle Screw System | |
30 | 00840996157315 | J070-0046 | HARRIER,SHORT ANT-LAT INSERTER SHEATH | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | HARRIER Choice Spine Intervertebral Body Device | |
31 | 00840996157308 | J070-0045 | HARRIER,SHORT INSERTER SHAFT | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | HARRIER Choice Spine Intervertebral Body Device | |
32 | 00840996150286 | 05-059-27-0000 | PROLIANT, COMPRESSOR | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Proliant Polyaxial Pedicle Screw System | |
33 | 00840996150262 | 05-059-12-0000 | PROLIANT, DRIVER, HEXALOBE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Proliant Polyaxial Pedicle Screw System | |
34 | 00840996150125 | J070-0038 | HARRIER,DISTRACTOR INSERTER | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | HARRIER Choice Spine Intervertebral Body Device | |
35 | 00840996148016 | SPCL-R1614805 | SPCL,TOMCAT,TRIAL,NO STOP,16x14x8 5H | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
36 | 00840996148009 | SPCL-R1614405 | SPCL,TOMCAT,TRIAL,NO STOP,16x14x4 5H | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
37 | 00840996147996 | SPCL-R1412805 | SPCL,TOMCAT,TRIAL,NO STOP,14x12x8 5H | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
38 | 00840996147989 | SPCL-R1412405 | SPCL,TOMCAT,TRIAL,NO STOP,14x12x4 5H | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
39 | 00840996147972 | SPCL-R008 | SPCL,TOMCAT,UNIVERSAL JOINT DRIVER,SPLI | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
40 | 00840996147965 | SPCL-R007 | SPCL,TOMCAT,ANGLED DRIVER GRIP | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
41 | 00840996147958 | SPCL-R006 | SPCL,TOMCAT,AWL,ANGLED,LONG | HWJ | AWL | 1 | TOMCAT™ Cervical Spinal System | |
42 | 00840996147941 | SPCL-R005 | SPCL,TOMCAT,AWL,STRAIGHT,LONG | HWJ | AWL | 1 | TOMCAT™ Cervical Spinal System | |
43 | 00840996147934 | SPCL-R004 | SPCL,TOMCAT,U-JOINT FORCEPS | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
44 | 00840996147927 | SPCL-R003 | SPCL,TOMCAT,STP,MODIFIED | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
45 | 00840996147910 | SPCL-R002 | SPCL,TOMCAT,16X14 RASP,STOP REMOVED | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
46 | 00840996147903 | SPCL-R001 | SPCL,TOMCAT,14X12 RASP,STOP REMOVED | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
47 | 00840996146234 | R070-0020 | TOMCAT,TAMP | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
48 | 00840996146227 | R070-0019 | TOMCAT,DRIVER,U-JOINT,SPLIT TIP | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
49 | 00840996146210 | R070-0018 | TOMCAT,DRIVER,SPLIT TIP | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System | |
50 | 00840996136167 | R070-Z112 | TOMCAT,0P GUIDE,TABS, 12 HEIGHT | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | TOMCAT™ Cervical Spinal System |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00813210022300 | 800-0235 | Polyaxial Plate Inserter | primaLOK SP | WENZEL SPINE, INC. | |
2 | 00813210022294 | 800-0233 | Post Plate Inserter | primaLOK SP | WENZEL SPINE, INC. | |
3 | 00813210022287 | 800-0228 | Offset Provisional Locker | primaLOK SP | WENZEL SPINE, INC. | |
4 | 00813210022270 | 800-0227 | Inserter Compressor II | primaLOK SP | WENZEL SPINE, INC. | |
5 | 00813210022263 | 800-0203 | Removal Tool | primaLOK SP | WENZEL SPINE, INC. | |
6 | 00813210022256 | 800-0201 | Lock Ring Compressor | primaLOK SP | WENZEL SPINE, INC. | |
7 | 00813210022249 | 800-0200 | Implant Inserter | primaLOK SP | WENZEL SPINE, INC. | |
8 | 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. | |
9 | 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. | |
10 | 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. | |
11 | 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. | |
12 | 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. | |
13 | 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. | |
14 | 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. | |
15 | 00813210021365 | 800-0501 | Auxiliary Instrument Case | primaLOK SP | WENZEL SPINE, INC. | |
16 | 00813210021358 | 800-0500 | Instrument Case | primaLOK SP | WENZEL SPINE, INC. | |
17 | 00812352021318 | 4302081 | Royal Oak Pedicle Screw Instrument Set Case 2 | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
18 | 00812352021301 | 4301081 | Royal Oak Pedicle Screw Instrument Set Case 1 | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
19 | 00812352020564 | SR5.5-90 | Straight Rod Ø5.5x90mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
20 | 00812352020557 | SR5.5-80 | Straight Rod Ø5.5x80mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
21 | 00812352020540 | SR5.5-70 | Straight Rod Ø5.5x70mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
22 | 00812352020533 | SR5.5-50 | Straight Rod Ø5.5x50mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
23 | 00812352020526 | SR5.5-400 | Straight Rod Ø5.5 x 400mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
24 | 00812352020519 | SR5.5-40 | Straight Rod Ø5.5x40mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
25 | 00812352020502 | SR5.5-200 | Straight Rod Ø5.5x200mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
26 | 00812352020496 | SR5.5-180 | Straight Rod Ø5.5x180mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
27 | 00812352020489 | SR5.5-150 | Straight Rod Ø5.5x150mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
28 | 00812352020472 | SR5.5-120 | Straight Rod Ø5.5x120mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
29 | 00812352020465 | SR5.5-110 | Straight Rod Ø5.5x110mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
30 | 00812352020458 | SR5.5-100 | Straight Rod Ø5.5x100mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
31 | 00812352020441 | PS5.5-7.5-55 | 5.5mm Pedicle Screw Assembly Ø7.5x55mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
32 | 00812352020434 | PS5.5-7.5-50 | 5.5mm Pedicle Screw Assembly Ø7.5x50mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
33 | 00812352020427 | PS5.5-7.5-45 | 5.5mm Pedicle Screw Assembly Ø7.5x45mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
34 | 00812352020410 | PS5.5-7.5-40 | 5.5mm Pedicle Screw Assembly Ø7.5x40mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
35 | 00812352020403 | PS5.5-7.5-35 | 5.5mm Pedicle Screw Assembly Ø7.5x35mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
36 | 00812352020397 | PS5.5-7.5-30 | 5.5mm Pedicle Screw Assembly Ø7.5x30mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
37 | 00812352020380 | PS5.5-6.5-55 | 5.5mm Pedicle Screw Assembly Ø6.5x55mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
38 | 00812352020373 | PS5.5-6.5-50 | 5.5mm Pedicle Screw Assembly Ø6.5x50mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
39 | 00812352020366 | PS5.5-6.5-45 | 5.5mm Pedicle Screw Assembly Ø6.5x45mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
40 | 00812352020359 | PS5.5-6.5-40 | 5.5mm Pedicle Screw Assembly Ø6.5x40mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
41 | 00812352020342 | PS5.5-6.5-35 | 5.5mm Pedicle Screw Assembly Ø6.5x35mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
42 | 00812352020335 | PS5.5-6.5-30 | 5.5mm Pedicle Screw Assembly Ø6.5x30mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
43 | 00812352020328 | PS5.5-5.5-50 | 5.5mm Pedicle Screw Assembly Ø5.5x50mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
44 | 00812352020311 | PS5.5-5.5-45 | 5.5mm Pedicle Screw Assembly Ø5.5x45mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
45 | 00812352020304 | PS5.5-5.5-40 | 5.5mm Pedicle Screw Assembly Ø5.5x40mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
46 | 00812352020298 | PS5.5-5.5-35 | 5.5mm Pedicle Screw Assembly Ø5.5x35mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
47 | 00812352020281 | PS5.5-4.5-50 | 5.5mm Pedicle Screw Assembly Ø4.5x50mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
48 | 00812352020274 | PS5.5-4.5-45 | 5.5mm Pedicle Screw Assembly Ø4.5x45mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
49 | 00812352020267 | PS5.5-4.5-40 | 5.5mm Pedicle Screw Assembly Ø4.5x40mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC | |
50 | 00812352020250 | PS5.5-4.5-35 | 5.5mm Pedicle Screw Assembly Ø4.5x35mm | Royal Oak Pedicle Screw System | ROYAL OAK MEDICAL DEVICES LLC |