BIOPRO ZIRALLOY MODULAR FEMORAL HEADS

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS is an FDA 510(k)-cleared medical device (K912641) 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 November 26, 1991. Regulation: 8.