Reliance Medical Systems
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2019-01-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K181118 | Reliance Lumbar IBF System | OVD | 2019-01-09 | View |
| 510(k) | K180687 | Reliance Lumber IBF System | MAX | 2018-05-15 | View |
No matching devices.