Kalitec Medical, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K220902 | Navagio Lumbar Cage | MAX | 2022-05-27 | View |
| 510(k) | K182210 | TiWAVE-L Porous Titanium Lumbar Cage | MAX | 2019-01-07 | View |
No matching devices.
Advertisement