Foundation Surgical Group, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2026-04-16
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K260011 | Foundation Surgical Navigated Lateral Disc Prep Instruments | OLO | 2026-04-16 | View |
| 510(k) | K241468 | Vertiwedge® Intraosseous System | MQP | 2024-11-07 | View |
| 510(k) | K241487 | Interwedge® Standalone Lateral | OVD | 2024-10-02 | View |
No matching devices.