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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.
 
DevicePASCAL Precision Transcatheter Valve Repair System (Implant System), PASCAL Precision Transcatheter Valve Repair System
Generic NameMitral valve repair devices
ApplicantEdwards Lifesciences, LLC
One Edwards Way
Irvine, CA 92614
PMA NumberP220003
Supplement NumberS009
Date Received05/01/2023
Decision Date05/31/2023
Product Code NKM 
Advisory Committee Cardiovascular
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for a sterilization site located at the STERIS, Synergy Health Ireland Limited Facility, IDA Business & Technology Park, Sragh Industrial Estate, Tullamore, Co. Offaly, R35 X865 Ireland for the sterilization of the PASCAL Precision Transcatheter Valve Repair System including the PASCAL Precision implant system (Models 20000IS and 20000ISM) and the PASCAL Precision guide sheath (Model 20000GS).
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