MicroPort CoCr Femoral Heads

MicroPort CoCr Femoral Heads is an FDA 510(k)-cleared medical device (K190123) manufactured by Microport Orthopedics, 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 July 14, 2019. Regulation: 8.