
Spinefrontier, Inc.
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DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031 is an FDA 510(k)-cleared medical device (K091638) manufactured by Spinefrontier, 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 September 13, 2009. Regulation: 8.