Foundation Surgical Group
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-07-31
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261810 | Vertiwedge® Intraosseous System | MQP | 2026-07-31 | View |
| 510(k) | K261809 | Interwedge® Standalone Lateral | OVD | 2026-07-31 | View |
No matching devices.