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Synthes USA Products, LLC
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SYNTHES MULTILOC HUMERAL NAILING SYSTEM is an FDA 510(k)-cleared medical device (K120807) manufactured by Synthes USA Products, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 5, 2012. Regulation: 8.