Reprocessed Shavers/Burs

Reprocessed Shavers/Burs is an FDA 510(k)-cleared medical device (K172092) manufactured by Renovo, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 2017. Regulation: 8.