FDA 510(k), K946106, GORE-TEX DUALMESH PLUS BIOMATERIAL

FDA 510(k), K946106, GORE-TEX DUALMESH PLUS BIOMATERIAL

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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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