Renovo, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Reprocessed DePuy Mitek Ablation Wand, Reprocessed ArthoCare Ablation Wand, Reprocessed ArthroCare ENT Coblator
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Renovo, Inc. Orthopedic ✕
1 devices