22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD

22.2/+4MM CO CR & ZIRCONIA FEMORAL HEAD is an FDA 510(k)-cleared medical device (K970846) manufactured by Landos, 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 June 4, 1997. Regulation: 8.