TILLMAN HIPSURFACE REPLACEMENT

TILLMAN HIPSURFACE REPLACEMENT is an FDA 510(k)-cleared medical device (K781490) manufactured by Waldemar Link GmbH & Co. KG. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 19, 1978. Regulation: 8.