INTERPLANTA SP TOTAL HIP PROSTHESIS

INTERPLANTA SP TOTAL HIP PROSTHESIS is an FDA 510(k)-cleared medical device (K790488) 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 March 27, 1979. Regulation: 8.