CEMENTED CALCAR REPLACEMENT FEMORAL STEM

CEMENTED CALCAR REPLACEMENT FEMORAL STEM is an FDA 510(k)-cleared medical device (K964795) manufactured by Johnson & Johnson Professionals, 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 18, 1997. Regulation: 8.