Medtronic Inc 710 Medtronic Parkway Neminneapolis Mn 55432 Pma Numberp080006 Supplement Numbers171 Date Received04 27 2022 Decision Date05 03 2022 Product Code Ojx 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 Parkway Neminneapolis Mn 55432 Pma Numberp080006 Supplement Numbers171 Date Received04 27 2022 Decision Date05 03 2022 Product Code Ojx 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 P080006S171 MEDTRONIC Inc.710 Medtronic Parkway Neminneapolis, MN 55432 PMA NumberP080006 Supplement NumberS171 Date Received04/27/2022 Decision Date05/03/2022 Product Code OJX  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Attain Performa Lead, Attain Stability Quad MRI Lead	2022-05-03