ARAGON SURGICAL RF SYSTEM L2 INSTRUMENT

ARAGON SURGICAL RF SYSTEM L2 INSTRUMENT is an FDA 510(k)-cleared medical device (K090306) manufactured by Aragon Surgical, 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 June 17, 2009. Regulation: 8.