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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.
 
DeviceMEDTRONIC CARELINK MONITOR MODEL 2490C, CARDIOSIGHT READER
Generic NamePacemaker/icd/crt non-implanted components
ApplicantMedtronic, Inc.
8200 CORAL SEA STREET N.E.
MOUNDS VIEW, MN 55112
PMA NumberP890003
Supplement NumberS181
Date Received12/23/2009
Decision Date11/09/2011
Product Code OSR 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Review MemoReview Memo
RecallsCDRH Recalls
Approval Order Statement  
APPROVAL FOR THE PROTECTA XT CRT-D, D314TRM AND PROTECTA CRT-DD334TRM IMPLANTABLE CARDIOVERTCR DEFIBRILLATORS WITH CARDIAC RCSYNCHRONIZATION, PROTECTA XT DR D314DRM AND PROTECTA DR D334DRM IMPLANTABLE CARDIOVERTER DEFIBRILLAIORS, MODEL SW009 APPLICATION SOFTWARE VL.0, CARELINK MONITOR MODEL 2490C UPGRADE. CARDIOSIGHT READER MODEL 2020A UPGRADE AND MODEL 2491 DDMA UPGRADE.
Approval OrderApproval Order
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