
Aesculap Implant Systems
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AESCULAP IMPLANT SYSTEMS S4 SPINAL SYSTEM is an FDA 510(k)-cleared medical device (K100623) manufactured by Aesculap Implant Systems. 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 8, 2010. Regulation: 8.