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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.
 
DeviceCONTAK RENEWAL 3 AVT CRT-D
Generic NameImplantable pulse generator, pacemaker (non-CRT)
ApplicantBoston Scientific Corp.
4100 HAMLINE AVE NORTH
ST. PAUL, MN 55112
PMA NumberP010012
Supplement NumberS175
Date Received03/01/2008
Decision Date03/17/2008
Product Code LWP 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR THE SYSTEM SOFTWARE MODEL 2909 V6.02 WITH THE PROGRAMMER MODEL 3120 AND THE MODEL 2893 APPLICATION SOFTWARE FOR THE CONTAK RENEWAL 3 AVT PULSE GENERATORS (MODELS M150, M155, M157 AND M159).
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