Reprocessed DePuy Mitek Ablation Wand

Reprocessed DePuy Mitek Ablation Wand is an FDA 510(k)-cleared medical device (K173740) manufactured by Renovo, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2018. Regulation: 8.