BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED is an FDA 510(k)-cleared medical device (K925682) manufactured by Biopro, 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 6, 1994. Regulation: 8.