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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 K101587
Device Name PROPATCH SOFT TISSUE REPAIR MATRIX
Original Applicant
CRYOLIFE, INC.
1655 roberts blvd., n.w.
kennesaw,  GA  30144
Original Contact bryan brosseau
Regulation Number878.3300
Classification Product Code
FTM  
Subsequent Product Codes
OWY   OXB   OXE   OXH   OXK  
Date Received06/08/2010
Decision Date 09/16/2010
Decision substantially equivalent (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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