ARTHROSCOPE / MEDIFIX INC.

ARTHROSCOPE / MEDIFIX INC. is an FDA 510(k)-cleared medical device (K992474) manufactured by Medifix, 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 September 22, 1999. Regulation: 8.