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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 NameDIVA FAMILY, SELECTION AFM C-SERIES AND T-SERIES DEVICES
Classification Nameimplantable cardioverter defibrillator (non-crt)
Applicant MEDTRONIC INC.
PMA NumberP980050
Supplement NumberS073
Date Received04/04/2012
Decision Date04/25/2012
Product Code
LWS[ Registered Establishments with LWS ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for software updates and minor software enhancements to medtronic model 9986 desktop/ baseline operating system software (boss) version 2. 6 for the medtronic model 2090 carelink programmer.
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