AESCULAP SPINE SYSTEM ADDITIONAL COMPONENTS

AESCULAP SPINE SYSTEM ADDITIONAL COMPONENTS is an FDA 510(k)-cleared medical device (K980121) 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 9, 1998. Regulation: 8.