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Meditech Advisors, LLC
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TALOS INTERVERTEBRAL BODY FUSION DEVICE is an FDA 510(k)-cleared medical device (K090707) manufactured by Meditech Advisors, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 14, 2009. Regulation: 8.