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X-Spine Systems, Inc.
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FORTEX PEDICLE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K120832) manufactured by X-Spine Systems, Inc.. 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 22, 2012. Regulation: 8.