ARTHROSCOPIC ELECTROSURGICAL PROBE

ARTHROSCOPIC ELECTROSURGICAL PROBE is an FDA 510(k)-cleared medical device (K901505) 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 April 17, 1990. Regulation: 8.