ARTHRO-SURGIMAT

ARTHRO-SURGIMAT is an FDA 510(k)-cleared medical device (K962114) manufactured by W.O.M. World of Medicine 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 August 21, 1996. Regulation: 8.