Spinefrontier, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2020-06-19
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K193106 | SpineFrontier Lumbar Interbody Fusion Device System | MAX | 2020-06-19 | View |
| 510(k) | K172484 | A-CIFT SoloFuse | OVE | 2018-05-08 | View |
No matching devices.