DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION

DYONICS DISPOSABLE ARTHROSCOPIC SURGERY BLADES MODIFICATION is an FDA 510(k)-cleared medical device (K934299) 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 February 13, 1994. Regulation: 8.