ARTHRO-SURGIMAT-2000 ECU

ARTHRO-SURGIMAT-2000 ECU is an FDA 510(k)-cleared medical device (K990443) 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 25, 1999. Regulation: 8.