Synthes USA Products, LLC - FDA 510(k) Cleared Devices
Recent clearances: MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction System, SyntheCel Dura Repair, MAXFRAME Multi-Axial Correction System (aka MAXFRAME)
61
Total
61
Cleared
0
Denied
FDA 510(k) Regulatory Record - Synthes USA Products, LLC General Hospital ✕
1 devices