MODIFICATON TO: ARTHROCARE ARTHROWANDS

MODIFICATON TO: ARTHROCARE ARTHROWANDS is an FDA 510(k)-cleared medical device (K072865) manufactured by Arthrocare Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 22, 2007. Regulation: 8.