
Kensey Nash Corp.
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MEDEOR MATRIX, MODELS 30010-XX (HYDRATED); 30020-XX (DRY) is an FDA 510(k)-cleared medical device (K091499) manufactured by Kensey Nash Corp.. 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 October 21, 2009. Regulation: 8.