ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970)

ARTHROCARE ARTHROSCOPIC ELECTROSURGERY SYSTEM (MODEL 970) is an FDA 510(k)-cleared medical device (K961747) 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 July 14, 1996. Regulation: 8.