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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.
 
DeviceIngevity Lead Family (passive fixation models)
Generic NameImplantable pulse generator, pacemaker (non-CRT)
ApplicantBOSTONSCIENTIFIC
4100 HAMLINE AVENUE NORTH
ST PAUL, MN 55112
PMA NumberP150012
Supplement NumberS069
Date Received12/20/2018
Decision Date01/10/2019
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  
Change the authorized laboratory for testing USP grade polyethylene glycol (PEG) 3350 and mannitol material to other service providers.
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