Foundation Surgical Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Foundation Surgical Navigated Lateral Disc Prep Instruments, Vertiwedge® Intraosseous System, Interwedge® Standalone Lateral
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Foundation Surgical Group, Inc. Orthopedic ✕
3 devices