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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
510(k) Number K011025
Device Name FORTAFLEX SURGICAL MESH
Applicant
ORGANOGENESIS, INC.
150 DAN RD.
CANTON,  MA  02021
Applicant Contact PATRICK R BILBO
Correspondent
ORGANOGENESIS, INC.
150 DAN RD.
CANTON,  MA  02021
Correspondent Contact PATRICK R BILBO
Regulation Number878.3300
Classification Product Code
FTM  
Date Received04/05/2001
Decision Date 08/24/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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