REPROCESSED RF ARTHROSCOPY PROBES

REPROCESSED RF ARTHROSCOPY PROBES is an FDA 510(k)-cleared medical device (K012679) manufactured by Sterilmed, 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 November 7, 2001. Regulation: 8.