AESCULAP CRANIOFIX TITANIUM CLAMP SYSTEM

AESCULAP CRANIOFIX TITANIUM CLAMP SYSTEM is an FDA 510(k)-cleared medical device (K972332) manufactured by Aesculap, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 1998. Regulation: 8.