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Reliance Medical Systems, LLC
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RELIANCE POSTERIOR CERVICAL- THORACIC SYSTEM is an FDA 510(k)-cleared medical device (K122292) manufactured by Reliance Medical Systems, 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 October 23, 2012. Regulation: 8.