| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00190837003630 | 80-3830-0617 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 2 | 00190837003678 | 80-3830-1217 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 3 | 00190837003661 | 80-3830-1215 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 4 | 00190837003654 | 80-3830-1213 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 5 | 00190837003647 | 80-3830-1211 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 6 | 00190837003623 | 80-3830-0615 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 7 | 00190837003616 | 80-3830-0613 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 8 | 00190837003609 | 80-3830-0611 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 9 | 00190837003593 | 80-3226-1217 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 10 | 00190837003586 | 80-3226-1215 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 11 | 00190837003579 | 80-3226-1213 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 12 | 00190837003562 | 80-3226-1211 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 13 | 00190837003555 | 80-3226-0617 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 14 | 00190837003548 | 80-3226-0615 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 15 | 00190837003531 | 80-3226-0613 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 16 | 00190837003524 | 80-3226-0611 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 17 | 00190837003517 | 80-155-30 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 18 | 00190837003500 | 80-155-25 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 19 | 00190837003494 | 80-155-20 | OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 2 | Dyna-Link Stand-Alone Anterior Lumbar System | ||
| 20 | 00190837137106 | 132-2314-2 | PEK | Spinous Process Plate | 2 | Aileron TRX | ||
| 21 | 00190837137090 | 132-2308-2 | PEK | Spinous Process Plate | 2 | Aileron TRX | ||
| 22 | 00190837098230 | 132-1-131 | 132-1-131 | PEK | Spinous process plate | 2 | Aileron Static | |
| 23 | 00190837094607 | 113-726 | 113-726 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 24 | 00190837094591 | 113-547 | 113-547 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 25 | 00190837094034 | 113-1444 | 113-1444 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 26 | 00190837093846 | 113-1744 | 113-1744 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 27 | 00190837093839 | 113-1743 | 113-1743 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 28 | 00190837093822 | 113-1742 | 113-1742 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 29 | 00190837093815 | 113-1741 | 113-1741 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 30 | 00190837093808 | 113-1740 | 113-1740 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 31 | 00190837093792 | 113-1739 | 113-1739 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 32 | 00190837093785 | 113-1738 | 113-1738 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 33 | 00190837093778 | 113-1737 | 113-1737 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 34 | 00190837093761 | 113-1736 | 113-1736 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 35 | 00190837093754 | 113-1735 | 113-1735 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 36 | 00190837093747 | 114-1444 | 114-1444 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 37 | 00190837093730 | 113-1443 | 113-1443 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 38 | 00190837093723 | 113-1442 | 113-1442 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 39 | 00190837093716 | 113-1441 | 113-1441 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 40 | 00190837093709 | 113-1440 | 113-1440 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 41 | 00190837093693 | 113-1439 | 113-1439 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 42 | 00190837093686 | 113-1438 | 113-1438 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 43 | 00190837093679 | 113-1437 | 113-1437 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 44 | 00190837093662 | 113-1436 | 113-1436 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 45 | 00190837093655 | 113-1435 | 113-1435 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 46 | 00190837093648 | 113-1044 | 113-1044 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 47 | 00190837093631 | 113-1043 | 113-1043 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 48 | 00190837093624 | 113-1042 | 113-1042 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 49 | 00190837093617 | 113-1038 | 113-1038 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C | |
| 50 | 00190837093600 | 113-1036 | 113-1036 | ODP | Intervertebral fusion device with bone graft, cervical | 2 | Plateau C |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00816728021520 | A175WTSE | A175WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 2 | 00816728021513 | A175WSE | A175WSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 3 | 00816728021506 | A175TSE | A175TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 4 | 00816728021490 | 175mm Retractor | A175SE | LT Adapt Smoke Evacuation Retractor, 175mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 5 | 00816728021483 | A155WTSE | A155WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 6 | 00816728021476 | A155WSE | A155WSE | LT Adapt Smoke Evacuation Retractor, 155mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 7 | 00816728021469 | A155TSE | A155TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 8 | 00816728021452 | 155mm Retractor | A155SE | LT Adapt Smoke Evacuation Retractor, 155mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 9 | 00816728021445 | A135WTSE | A135WTSE | LT Adapt Smoke Evacuation Retractor, 135mm, Wide, Teeth | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 10 | 00816728021438 | A135WSE | A135WSE | LT Adapt Smoke Evacuation Retractor, 135mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 11 | 00816728021421 | A135TSE | A135TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 12 | 00816728021414 | 135mm Retractor | A135SE | LT Adapt Smoke Evacuation Retractor, 135mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 13 | 00816728021407 | A90WTSE | A90WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 14 | 00816728021391 | A90WSE | A90WSE | LT Adapt Smoke Evacuation Retractor, 90mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 15 | 00816728021384 | A90TSE | A90TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
| 16 | 00816728021377 | 90mm Retractor | A90SE | LT Adapt Smoke Evacuation Retractor, 90mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
| 17 | 00816728021032 | C80R | C80R | LT Retractor, Rich, 80mm x 60mm | Eikon | STRYKER CORPORATION |
| 18 | 00816728021025 | C60R | C60R | LT Retractor, Rich, 60mm x 45mm | Eikon | STRYKER CORPORATION |
| 19 | 00816728021018 | C40R | C40R | LT Retractor, Rich, 40mm x 38mm | Eikon | STRYKER CORPORATION |
| 20 | 00816728021001 | C3550AN | C3550AN | LT Retractor, A-N, 35mm & 50mm | Eikon | STRYKER CORPORATION |
| 21 | 00816728020974 | 11109 | 11109 | Glenoid Retractor | N/A | STRYKER CORPORATION |
| 22 | 00816728020967 | E1SL | E1SL | Retractor, Standard, Long | Eiberg | STRYKER CORPORATION |
| 23 | 00816728020950 | E1S | E1S | Retractor, Standard | Eiberg | STRYKER CORPORATION |
| 24 | 00816728020844 | C175T | C175T | LT Retractor, 175 mm, Teeth | Eikon | STRYKER CORPORATION |
| 25 | 00816728020837 | C175 | C175 | LT Retractor, 175mm | Eikon | STRYKER CORPORATION |
| 26 | 00816728020820 | C135SH | C135SH | LT Retractor, 135mm, Sweetheart | Eikon | STRYKER CORPORATION |
| 27 | 00816728020813 | C135W | C135W | LT Retractor, 135mm, Wide | Eikon | STRYKER CORPORATION |
| 28 | 00816728020806 | C135WT | C135WT | LT Retractor, 135mm, Wide, Teeth | Eikon | STRYKER CORPORATION |
| 29 | 00816728020790 | C135T | C135T | LT Retractor, 135 mm, Teeth | Eikon | STRYKER CORPORATION |
| 30 | 00816728020783 | C135NT | C135NT | LT Retractor, 135 mm, Narrow, Teeth | Eikon | STRYKER CORPORATION |
| 31 | 00816728020776 | C135 | C135 | LT Retractor, 135 mm | Eikon | STRYKER CORPORATION |
| 32 | 00816728020769 | C135N | C135N | LT Retractor, 135mm, Narrow | Eikon | STRYKER CORPORATION |
| 33 | 00816728020752 | C90W | C90W | LT Retractor, 90 mm, Wide | Eikon | STRYKER CORPORATION |
| 34 | 00816728020745 | C90WT | C90WT | LT Retractor, 90 mm, Wide, Teeth | Eikon | STRYKER CORPORATION |
| 35 | 00816728020738 | C90T | C90T | LT Retractor, 90mm, Teeth | Eikon | STRYKER CORPORATION |
| 36 | 00816728020721 | C90NT | C90NT | LT Retractor, 90mm, Narrow, Teeth | Eikon | STRYKER CORPORATION |
| 37 | 00816728020714 | C90N | C90N | LT Retractor, 90mm, Narrow | Eikon | STRYKER CORPORATION |
| 38 | 00816728020707 | C90 | C90 | LT Retractor, 90mm | Eikon | STRYKER CORPORATION |
| 39 | 00816728020691 | C50T | C50T | LT Retractor, 50 mm, Teeth | Eikon | STRYKER CORPORATION |
| 40 | 00816728020684 | C50 | C50 | LT Retractor, 50 mm | Eikon | STRYKER CORPORATION |
| 41 | 00816728020677 | C40N | C40N | LT Retractor, 40mm, Narrow | Eikon | STRYKER CORPORATION |
| 42 | 00816728020660 | C40XN | C40XN | LT Retractor, 40 mm, Extra Narrow | Eikon | STRYKER CORPORATION |
| 43 | 00816728020554 | A38D | A38D | Deaver 38mm Wide Retractor | N/A | STRYKER CORPORATION |
| 44 | 00816728020547 | A25D | A25D | Deaver 25mm Wide Retractor | N/A | STRYKER CORPORATION |
| 45 | 00816728020493 | C3550ANXN | C3550ANXN | LT Retractor, A-N, 35mm & 50mm Extra Narrow | Eikon | STRYKER CORPORATION |
| 46 | 00816728020486 | C3550ANN | C3550ANN | LT Retractor, A-N, 35mm & 50mm Narrow | Eikon | STRYKER CORPORATION |
| 47 | 00812998040186 | LSTS-000022 | LSTS-000022 | 4WEB Medical | 4WEB MEDICAL | |
| 48 | 00812998032303 | PSTS-000501 | PSTS-000501 | 4WEB Medical | 4WEB MEDICAL | |
| 49 | 00812998032297 | PSTS-000500 | PSTS-000500 | 4WEB Medical | 4WEB MEDICAL | |
| 50 | 00812926029542 | 330-00-002 | Small Bone Distractor | TRILLIANT SURGICAL, LLC |