Medtronic Neuromodulation7000 Central Avenue Neminneapolis Mn 55432 Pma Numberp840001 Supplement Numbers513 Date Received03 02 2022 Decision Date03 30 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 Numbers513 Date Received03 02 2022 Decision Date03 30 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 P840001S513 MEDTRONIC NEUROMODULATION7000 Central Avenue Neminneapolis, MN 55432 PMA NumberP840001 Supplement NumberS513 Date Received03/02/2022 Decision Date03/30/2022 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® and Intellis Spinal Cord Stimulation Systems and Pisces, Specify®, and Vectris® Spinal	2022-03-30