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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 13 Results
Device Name: DualMesh Decision Date To: 04/27/2018
 
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Export all 13 Records to ExcelExport to Excel | Download Files | More About 510(k)
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gore dualmesh plus biomaterial gore mycromesh plus biomaterial W. L. GORE & ASSOCIATES, INC. K063435 11/28/2006
gore-tex dualmesh emerge plus biomaterial W. L. GORE & ASSOCIATES, INC. K032168 08/15/2003
dualmesh emerge & emerge plus biomaterial W.L. GORE & ASSOCIATES,INC K022782 09/10/2002
gore-tex dualmesh plus biomaterial with holes W.L. GORE & ASSOCIATES,INC K010228 02/21/2001
gore-tex dualmesh plus biomaterial (1 mm & 2mm) W.L. GORE & ASSOCIATES,INC K000185 02/14/2000
gore-tex dualmesh biomaterial W.L. GORE & ASSOCIATES,INC K992189 07/29/1999
soft tissue patch plus, dualmesh plus, mycromesh plus, dualmesh plus with holes W.L. GORE & ASSOCIATES,INC K981051 04/15/1998
gore-tex soft tissue patch plus/dualmesh plus biomaterial/mycromesh plus biomaterial/dualmesh plus biomaterial with hole W.L. GORE & ASSOCIATES,INC K965038 02/06/1997
gore-tex soft tissue patch,mycromesha biomaterial,dualmesh biomaterial,dualmesh biomaterial with holes W.L. GORE & ASSOCIATES,INC K963619 10/25/1996
gore-tex dualmesh plus biomaterial with holes W.L. GORE & ASSOCIATES,INC K962401 09/03/1996
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