CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.)

CASF (TM) (CONTOURED ANTERIOR SPINAL FIXATON SYS.) is an FDA 510(k)-cleared medical device (K904446) 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 September 4, 1991. Regulation: 8.