
Aesculap, Inc.
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AESCULAP CRANIOFACIAL PLATE AND SCREW is an FDA 510(k)-cleared medical device (K060492) manufactured by Aesculap, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 6, 2006. Regulation: 8.