BUCHALTER FAUSER FEMORAL COMPONENTS

BUCHALTER FAUSER FEMORAL COMPONENTS is an FDA 510(k)-cleared medical device (K952686) 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 September 18, 1995. Regulation: 8.