ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)

ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS) is an FDA 510(k)-cleared medical device (K873619) manufactured by Arthropedics, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 13, 1988. Regulation: 8.