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Tissue Regeneration Systems, Inc.
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TRS CRANIAL BONE VOID FILLER(TRS C-BVF) is an FDA 510(k)-cleared medical device (K123633) manufactured by Tissue Regeneration Systems, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 15, 2013. Regulation: 8.