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Conmed Linvatec
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CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURES is an FDA 510(k)-cleared medical device (K092898) manufactured by Conmed Linvatec. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 18, 2009. Regulation: 8.