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Synthes (Usa)
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SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS is an FDA 510(k)-cleared medical device (K111667) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 4, 2011. Regulation: 8.