
Rti Biologics, Inc.
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TUTOPATCH, TUTOMESH, MODELS 68350, 68351, 68352, 68353, 68354, 68355, 68356, 68357, 68358 is an FDA 510(k)-cleared medical device (K091142) manufactured by Rti Biologics, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 30, 2009. Regulation: 8.