ARGUS ARTHROSCOPY INSTRUMENT SYSTEM

ARGUS ARTHROSCOPY INSTRUMENT SYSTEM is an FDA 510(k)-cleared medical device (K950242) manufactured by Argus Medical Co., 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 14, 1995. Regulation: 8.