
Nu Vasive, Incorporated
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ARCHON ANTERIOR CERVICAL PLATE SYSTE, is an FDA 510(k)-cleared medical device (K122910) manufactured by Nu Vasive, Incorporated. 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 10, 2012. Regulation: 8.