Medtronic Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp960009 Supplement Numbers442 Date Received11 08 2022 Decision Date11 22 2022 Product Code Mhy Advisory Committee Neurology 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 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp960009 Supplement Numbers442 Date Received11 08 2022 Decision Date11 22 2022 Product Code Mhy Advisory Committee Neurology 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 P960009S442 MEDTRONIC Inc.7000 Central Avenue Neminneapolis, MN 55432-3576 PMA NumberP960009 Supplement NumberS442 Date Received11/08/2022 Decision Date11/22/2022 Product Code MHY  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™	2022-11-22