Medtronic Inc 710 Medtronic Parkway Neminneapolis Mn 55432 Pma Numberp080006 Supplement Numbers173 Date Received11 16 2022 Decision Date11 22 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 Numbers173 Date Received11 16 2022 Decision Date11 22 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 P080006S173 MEDTRONIC Inc.710 Medtronic Parkway Neminneapolis, MN 55432 PMA NumberP080006 Supplement NumberS173 Date Received11/16/2022 Decision Date11/22/2022 Product Code OJX  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Attain Ability Lead, Attain Performa Lead and Attain Stability Quad MRI Lead	2022-11-22