PARKE-DAVIS TOTAL HIP PROSTHESIS

PARKE-DAVIS TOTAL HIP PROSTHESIS is an FDA 510(k)-cleared medical device (K791875) manufactured by Warner-Lambert Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 1979. Regulation: 8.