ARTHROCARE 8000S COBLATOR SURGERY SYSTEM

ARTHROCARE 8000S COBLATOR SURGERY SYSTEM is an FDA 510(k)-cleared medical device (K053297) 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 5, 2005. Regulation: 8.