Medtronic Neuromodulation7000 Central Avenue Neminneapolis Mn 55432 Pma Numberp840001 Supplement Numbers536 Date Received01 20 2023 Decision Date02 02 2023 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 Numbers536 Date Received01 20 2023 Decision Date02 02 2023 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 P840001S536 MEDTRONIC NEUROMODULATION7000 Central Avenue Neminneapolis, MN 55432 PMA NumberP840001 Supplement NumberS536 Date Received01/20/2023 Decision Date02/02/2023 Product Code LGW  Advisory Committee Neurology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Restore and Itrel® Spinal Cord Stimulation Systems	2023-02-02