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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.
 
DeviceCAPSURE/CAPSURE SP/CAPSURE SP NOVUS/CAPSURE SENSE/VITATRON EXCELLENCE +/PS+/CRYSTALLINE
Generic NamePermanent defibrillator electrodes
ApplicantMedtronic Cardiac Rhythm Disease Management
8200 Coral Sea St. N.E
Mounds View, MN 55112
PMA NumberP830061
Supplement NumberS045
Date Received02/05/2009
Decision Date03/06/2009
Product Code NVY 
Advisory Committee Cardiovascular
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
ADDITION OF A SUPPLIER FOR AN EXTRUDED COMPONENT USED TO MANUFACTURE ADHESIVE.
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