PS3500 ARTHROSCOPIC SURGICAL SYSTEM

PS3500 ARTHROSCOPIC SURGICAL SYSTEM is an FDA 510(k)-cleared medical device (K892062) manufactured by Dyonics, 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 June 22, 1989. Regulation: 8.