MOTECH TITANIUM SURGICAL MESH

MOTECH TITANIUM SURGICAL MESH is an FDA 510(k)-cleared medical device (K900138) manufactured by Biedermann Motech GmbH. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 19, 1990. Regulation: 8.