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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameCARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS
Classification Namereplacement heart-valve
Generic Namebioprosthetic heart valve
Regulation Number870.3925
ApplicantEDWARDS LIFESCIENCES, LLC.
PMA NumberP860057
Supplement NumberS011
Date Received04/22/1999
Decision Date08/28/2000
Product Code
DYE[ Registered Establishments with DYE ]
Docket Number 00M-1483
Notice Date 09/11/2000
Advisory Committee Cardiovascular
Supplement Typepanel track
Supplement Reason location change: manufacturer
Expedited Review Granted? No
Combination Product No
Information About: Labeling, Approval Order, Summary of Safety and Effectiveness
Approval Order Statement 
Approval forthe carpentier-edwards perimount pericardial bioprosthesis model 6900 mitral, sizes 25, 27, 29, 31, and 33 mm. This device is indicated for patients who require replacement of their native or prosthetic mitral valve.
Approval Order Approval Order
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