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Maxim Surgical
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MAXIM SURGICAL X-TREME INTERBODY FUSION SYSTEM is an FDA 510(k)-cleared medical device (K123206) manufactured by Maxim Surgical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 6, 2013. Regulation: 8.