ZIRCONIA CERAMIC MODULAR HEADS(TYPE I TAPER) MODIF

ZIRCONIA CERAMIC MODULAR HEADS(TYPE I TAPER) MODIF is an FDA 510(k)-cleared medical device (K913420) 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 January 15, 1992. Regulation: 8.