OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM

OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM is an FDA 510(k)-cleared medical device (K962152) manufactured by Osteonics 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 August 13, 1996. Regulation: 8.