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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 K101851
Device Name VENTRALIGHT ST MESH
Applicant
DAVOL INC., SUB. C.R. BARD, INC.
100 CROSSINGS BLVD
WARWICK,  RI  02886
Applicant Contact MICHELLE GODIN
Correspondent
DAVOL INC., SUB. C.R. BARD, INC.
100 CROSSINGS BLVD
WARWICK,  RI  02886
Correspondent Contact MICHELLE GODIN
Regulation Number878.3300
Classification Product Code
FTL  
Date Received07/01/2010
Decision Date 07/15/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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