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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.
 
DeviceFRONTIER/FRONTIER II FAMILY OF CRT-PS
Generic NamePulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
ApplicantAbbott Medical
15900 Valley View Court
Sylmar, CA 91335
PMA NumberP030035
Supplement NumberS027
Date Received10/23/2006
Decision Date11/21/2006
Product Code NKE 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
ELIMINATION OF THE EXTRA PERIMETER STAKING EPOXY AT FINAL ASSEMBLY ON THE LV HYBRID AND COVER SUPPORT INTERFACE ON ALL AFFINITY, INTEGRITY, IDENTITY, VICTORY AND FRONTIER FAMILY OF DEVICES.
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