MODIFICATION OF ENCORE LINEAR POROUS COATED HIP

MODIFICATION OF ENCORE LINEAR POROUS COATED HIP is an FDA 510(k)-cleared medical device (K991325) manufactured by Encore Orthopedics, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 24, 1999. Regulation: 8.