KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS is an FDA 510(k)-cleared medical device (K974757) manufactured by Acromed 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 March 4, 1998. Regulation: 8.