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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 NamePARADYM AND PARADYM RF ICD (IMPLANTABLE CARDIOVERTER DEFIBRILLATOR)
Classification Namedefibrillator, implantable, dual-chamber
Generic Nameimplantable cardioverter-defibrillator with active housing
ApplicantSORIN CRM USA, INC.
PMA NumberP980049
Supplement NumberS076
Date Received07/06/2012
Decision Date07/31/2012
Product Code
MRM[ Registered Establishments with MRM ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change: packaging
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Update to the thermosealing process.
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