SCHOELLY ARTHROSCOPE

SCHOELLY ARTHROSCOPE is an FDA 510(k)-cleared medical device (K133682) manufactured by Scholly Fiberoptic GmbH. 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 1, 2014. Regulation: 8.