ARTHROCARE HEAD AND NECK COBLATION WAND

ARTHROCARE HEAD AND NECK COBLATION WAND is an FDA 510(k)-cleared medical device (K131205) manufactured by ArthroCare Corporation. 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 August 8, 2013. Regulation: 8.