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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mesh, Surgical, Polymeric
510(k) Number K022782
FOIA Releasable 510(k) K022782
Device Name DUALMESH EMERGE & EMERGE PLUS BIOMATERIAL
Applicant
W.L. GORE & ASSOCIATES,INC
301 AIRPORT RD
ELKTON,  MD  21922 -1408
Applicant Contact R. LARRY PRATT
Correspondent
W.L. GORE & ASSOCIATES,INC
301 AIRPORT RD
ELKTON,  MD  21922 -1408
Correspondent Contact R. LARRY PRATT
Regulation Number878.3300
Classification Product Code
FTL  
Date Received08/22/2002
Decision Date 09/10/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
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