Ldr Spine USA
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2016-03-31
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153495 | Avenue L Lateral Lumbar Cage, Avenue T TLIF Cage System, ROI-A ALIF Cage System, ROI-T Implant System | MAX | 2016-03-31 | View |
| 510(k) | K152137 | FacetBRIDGE System | MRW | 2016-01-25 | View |
No matching devices.