MODIFICATION TO ARTHROCARE ARTHROWANDS

MODIFICATION TO ARTHROCARE ARTHROWANDS is an FDA 510(k)-cleared medical device (K070958) 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 April 22, 2007. Regulation: 8.