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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.
 
DeviceMicrony family of Pacemakers
Generic NamePulse-generator, single chamber, sensor driven, implantable
ApplicantABBOTT MEDICAL
15900 Valley View Ct.
Sylmar, CA 91335
PMA NumberP970013
Supplement NumberS099
Date Received12/30/2025
Decision Date07/21/2026
Product Code LWO 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
approval for Merlin 2 Patient Care System (PCS) programmer support for the AVEIR Leadless Pacemakers.
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