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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.
 
DeviceCentriMag™ Circulatory Support System
Generic NameVentricular (assist) bypass
ApplicantAbbott
6035 Stoneridge Dr.
Pleasanton, CA 94588
PMA NumberP170038
Supplement NumberS029
Date Received02/02/2026
Decision Date04/17/2026
Product Code DSQ 
Advisory Committee Cardiovascular
Supplement TypeReal-Time Process
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for labeling changes to the CentriMag Motor Instructions for Use (IFU), CentriMag Blood Pump IFU, and CentriMag Circulatory Support System Operation Manual.
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