ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODIFICATION)

ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODIFICATION) is an FDA 510(k)-cleared medical device (K953659) 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 September 28, 1995. Regulation: 8.