KANEDA SR ANTERIOR SPINAL SYSTEM

KANEDA SR ANTERIOR SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K971248) 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 June 10, 1997. Regulation: 8.