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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 NameVENTAK AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (AICD) SYSTEM FAMILY
Classification Nameimplantable cardioverter defibrillator (non-crt)
ApplicantBOSTON SCIENTIFIC-CRM
PMA NumberP830060
Supplement NumberS070
Date Received03/26/2012
Decision Date04/23/2012
Product Code
LWS[ Registered Establishments with LWS ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Implementation of a new acceptance methodology at the quality system level.
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