
Allo Pro Corp.
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POLYETHYLENE MEDULLARY PLUG - STIIHMER/ is an FDA 510(k)-cleared medical device (K830949) manufactured by Allo Pro 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 April 11, 1983. Regulation: 8.