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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 NameHANCOCK MODIFIED ORIFICE (MO) VALVED CONDUIT, MODEL 150
Classification Nameheart-valve, non-allograft tissue
Generic Nameheart valve
ApplicantMEDTRONIC CARDIAC SURGERY, MEDTRONIC, INC.
PMA NumberP790007
Supplement NumberS017
Date Received12/27/2005
Decision Date04/20/2006
Product Code
LWR[ Registered Establishments with LWR ]
Advisory Committee Cardiovascular
Supplement Type135 review track for 30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the implementation of smaller capacity equipment and elimination of the shrink temperature testing used for the tissue fixation manufacturing process.
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