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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.
 
DeviceESSENTIO VALITUDE™ MRI: L110, L111, L131;PROPONENT VALITUDE™ MRI: L210, L211, L231; ACCOLADE VALITUDE™ MRI: L310, L311,
Generic NameImplantable pulse generator, pacemaker (non-CRT)
ApplicantBOSTONSCIENTIFIC
4100 HAMLINE AVENUE NORTH
ST PAUL, MN 55112
PMA NumberP150012
Supplement NumberS007
Date Received05/26/2016
Decision Date06/20/2016
Product Codes LWP NVN 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductYes
Approval Order Statement  
Remove the final finish wetblast manufacturing process step.
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