
Wrightmedicaltechnologyinc
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CHARLOTTE HIGH-DEMAND COMPRESSION SCREW is an FDA 510(k)-cleared medical device (K043281) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 18, 2005. Regulation: 8.