KINEMAX TIBIAL STEM EXTENSION

KINEMAX TIBIAL STEM EXTENSION is an FDA 510(k)-cleared medical device (K896452) manufactured by Howmedica Corp.. 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 3, 1990. Regulation: 8.