
Vilex, Inc.
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FUZE: INTRAMEDULLARY INTERNAL FIXATION NAIL is an FDA 510(k)-cleared medical device (K102413) manufactured by Vilex, 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 November 13, 2011. Regulation: 8.