ARTHREX ARTHROSCOPY ICE BLADE

ARTHREX ARTHROSCOPY ICE BLADE is an FDA 510(k)-cleared medical device (K921823) manufactured by Arthrex, 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 October 14, 1992. Regulation: 8.