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FDA 510(k) K946106, GORE-TEX DUALMESH PLUS BIOMATERIAL, by W. L. Gore & Associates, Inc.

FDA 510(k) K946106, GORE-TEX DUALMESH PLUS BIOMATERIAL, by W. L. Gore & Associates, Inc.

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510(K) Number: K946106
Device Name: GORE-TEX DUALMESH PLUS BIOMATERIAL
Manufacturer: W. L. Gore & Associates, Inc.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 12/14/1994
Decision Date: 04/24/1995
Regulation Medical Specialty: General & Plastic Surgery
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