
Sicat GmbH & Co. KG
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SICAT IMPLANT V1.2 is an FDA 510(k)-cleared medical device (K103723) manufactured by Sicat GmbH & Co. KG. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 19, 2011. Regulation: 8.