AESUCLAP SOCON SPINAL SYSTEM

AESUCLAP SOCON SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K970285) manufactured by Aesculap, Inc.. 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 24, 1997. Regulation: 8.