Arthocare Corporation - FDA 510(k) Cleared Devices
Recent clearances: MultiFIX S Ultra Knotless Fixation System, MULTIFIX S KNOTLESS FIXATION DEVICE, AMBIENT TURBOFLASH 90 IFS
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthocare Corporation Orthopedic ✕
3 devices