ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM MODEL 970 is an FDA 510(k)-cleared medical device (K943450) manufactured by Arthrocare Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 12, 1995. Regulation: 8.