LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT

LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT is an FDA 510(k)-cleared medical device (K984296) manufactured by Biomet, 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 February 17, 1999. Regulation: 8.