Medtronic Inc 710 Medtronic Parkwayminneapolis Mn 55432 Pma Numberp130021 Supplement Numbers119 Date Received07 20 2022 Decision Date08 03 2022 Product Code Npt Advisory Committee Cardiovascular Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Medtronic Inc 710 Medtronic Parkwayminneapolis Mn 55432 Pma Numberp130021 Supplement Numbers119 Date Received07 20 2022 Decision Date08 03 2022 Product Code Npt Advisory Committee Cardiovascular Supplement Type30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P130021S119 Medtronic, Inc.710 Medtronic Parkwayminneapolis,, MN 55432 PMA NumberP130021 Supplement NumberS119 Date Received07/20/2022 Decision Date08/03/2022 Product Code NPT  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Medtronic CoreValve Evolut R System, Medtronic CoreValve Evolut PRO System, Medtronic Evolut PRO+ System	2022-08-03