ARTHROCARE PERC-D SPINEWAND

ARTHROCARE PERC-D SPINEWAND is an FDA 510(k)-cleared medical device (K053447) 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 December 26, 2005. Regulation: 8.