Medtronic Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp960009 Supplement Numbers440 Date Received10 12 2022 Decision Date10 21 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 Numbers440 Date Received10 12 2022 Decision Date10 21 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 P960009S440 MEDTRONIC Inc.7000 Central Avenue Neminneapolis, MN 55432-3576 PMA NumberP960009 Supplement NumberS440 Date Received10/12/2022 Decision Date10/21/2022 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™	2022-10-21