SMITH & NEPHEW DYONICS TMJ ARTHROSCOPY INFLOW SET

SMITH & NEPHEW DYONICS TMJ ARTHROSCOPY INFLOW SET is an FDA 510(k)-cleared medical device (K914963) manufactured by Smith & Nephew 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 3, 1992. Regulation: 8.