NATURAL-KNEE II REVISION FEMORAL SPACER LUGS

NATURAL-KNEE II REVISION FEMORAL SPACER LUGS is an FDA 510(k)-cleared medical device (K970498) manufactured by Intermedics Orthopedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 29, 1997. Regulation: 8.