Arthrocare Corp. - FDA 510(k) Cleared Devices
Recent clearances: Adjustable Fixation Device, SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT, SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURATOR, LOW PROFILE DR
112
Total
112
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arthrocare Corp. Neurology ✕
1 devices