ARTHRO-SURGIMAT-A103

ARTHRO-SURGIMAT-A103 is an FDA 510(k)-cleared medical device (K000153) 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 February 7, 2000. Regulation: 8.