CANNULA MODEL AR-6001

CANNULA MODEL AR-6001 is an FDA 510(k)-cleared medical device (K880295) manufactured by Arthrex Arthroscopy Instruments, 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 June 28, 1988. Regulation: 8.