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FDA 510(k), K063435, GORE DUALMESH PLUS BIOMATERIAL GORE MYCROMESH PLUS BIOMATERIAL
FDA 510(k), K063435, GORE DUALMESH PLUS BIOMATERIAL GORE MYCROMESH PLUS BIOMATERIAL
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$149.00 USD
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$149.00 USD
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510(K) Number: K063435
Device Name: GORE DUALMESH PLUS BIOMATERIAL GORE MYCROMESH PLUS BIOMATERIAL
Manufacturer: W. L. GORE & ASSOCIATES, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 11/13/2006
Decision Date: 11/28/2006
Regulation Medical Specialty: General & Plastic Surgery
Device Name: GORE DUALMESH PLUS BIOMATERIAL GORE MYCROMESH PLUS BIOMATERIAL
Manufacturer: W. L. GORE & ASSOCIATES, INC.
Device Classification Name: mesh, surgical, polymeric
Regulation Number: 878.3300
Classification Product Code: FTL
Date Received: 11/13/2006
Decision Date: 11/28/2006
Regulation Medical Specialty: General & Plastic Surgery
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