Medtronic Neuromodulation7000 Central Avenue N E Minneapolis Mn 55432 Pma Numberp970004 Supplement Numbers373 Date Received08 31 2022 Decision Date09 13 2022 Product Code Ezw Advisory Committee Gastroenterology Urology 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 N E Minneapolis Mn 55432 Pma Numberp970004 Supplement Numbers373 Date Received08 31 2022 Decision Date09 13 2022 Product Code Ezw Advisory Committee Gastroenterology Urology 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 P970004S373 MEDTRONIC NEUROMODULATION7000 Central Avenue, N.e.minneapolis, MN 55432 PMA NumberP970004 Supplement NumberS373 Date Received08/31/2022 Decision Date09/13/2022 Product Code EZW  Advisory Committee Gastroenterology/Urology Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	InterStim® Therapy System, Verify® Evaluation System	2022-09-13