
Renovo, Inc.
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Reprocessed ArthoCare Ablation Wand is an FDA 510(k)-cleared medical device (K173741) 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 4, 2018. Regulation: 8.