OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIES

OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIES is an FDA 510(k)-cleared medical device (K953913) manufactured by Optus, 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 January 21, 1996. Regulation: 8.