MITEK ELECTROSURGICAL SYSTEM FOR ARTHROSCOPIC USE

MITEK ELECTROSURGICAL SYSTEM FOR ARTHROSCOPIC USE is an FDA 510(k)-cleared medical device (K963783) manufactured by ETHICON, 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 24, 1996. Regulation: 8.