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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.
 
DeviceINCEPTA, ENERGEN, PUCTUA, COGNIS, DYANAGEN, INOGEN, ORIGEN CRT-DS
Generic NameImplantable pulse generator, pacemaker (non-CRT)
ApplicantBoston Scientific Corp
4100 Hamline Ave. N
St Paul, MN 55112
PMA NumberP010012
Supplement NumberS358
Date Received06/09/2014
Decision Date07/08/2014
Product Code LWP 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
ADD A FUNCTIONALLY EQUIVALENT STERILIZATION CHAMBER; 2) ADD A THIRD ABATOR TO BE USED WITH THE ADDITIONAL STERILIZER; AND 3) INCLUDE STERILIZER CHAMBER ENHANCEMENTS REQUIRED FOR THE EXISTING AND ADDITIONAL STERILIZER CHAMBERS.
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