
Kensey Nash Corp.
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IMPRO VISE ABSORBABLE CEMENT FLOW RESTRICTOR is an FDA 510(k)-cleared medical device (K011943) 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 September 18, 2001. Regulation: 8.