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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceMITROFLOW AORTIC PERICARDIAL HEART VALVE
Generic Nameheart-valve, non-allograft tissue
ApplicantCORCYM Canada Corp.
5005 North Fraser Way
Burnaby V5J 5
PMA NumberP060038
Supplement NumberS005
Date Received07/08/2009
Decision Date08/07/2009
Withdrawal Date 10/17/2022
Product Code LWR 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
CHANGE IN THE MINIMUM EXPOSURE TIME FOR THE STERILIZATION PROCESS OF THE DEVICE.
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