EDWARDS DISPOSABLE ARTHROSCOPY CANNULA

EDWARDS DISPOSABLE ARTHROSCOPY CANNULA is an FDA 510(k)-cleared medical device (K884301) manufactured by Baxter Healthcare Corp. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1989. Regulation: 8.