
Kmi Kolster Methods, Inc.
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KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE is an FDA 510(k)-cleared medical device (K060414) manufactured by Kmi Kolster Methods, 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 October 22, 2006. Regulation: 8.