Medtronic Neuromodulation7000 Central Avenue Neminneapolis Mn 55432 Pma Numberp840001 Supplement Numbers532 Date Received11 08 2022 Decision Date11 22 2022 Product Code Lgw 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 Neuromodulation7000 Central Avenue Neminneapolis Mn 55432 Pma Numberp840001 Supplement Numbers532 Date Received11 08 2022 Decision Date11 22 2022 Product Code Lgw 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 P840001S532 MEDTRONIC NEUROMODULATION7000 Central Avenue Neminneapolis, MN 55432 PMA NumberP840001 Supplement NumberS532 Date Received11/08/2022 Decision Date11/22/2022 Product Code LGW  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Master Restore, Itrel®, Synergy®, Intellis and Vanta Spinal Cord Stimulation Systems and Pisces, Specify®, and Vectris®	2022-11-22