Medtronic Sofamor Danek USA, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: KYPHON HV-R Fenestrated Screw Cement, CD HORIZON Fenestrated Screw Set, CD HORIZON Growth Rod Conversion Set
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic Sofamor Danek USA, Incorporated Orthopedic ✕
2 devices