OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPES

OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPES is an FDA 510(k)-cleared medical device (K945267) 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 May 22, 1995. Regulation: 8.