Medtronic Neuromodulation7000 Central Avenue Nems Rcw225minneapolis Mn 55432 Pma Numberp080025 Supplement Numbers266 Date Received07 20 2022 Decision Date07 28 2022 Product Code Qon 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 Nems Rcw225minneapolis Mn 55432 Pma Numberp080025 Supplement Numbers266 Date Received07 20 2022 Decision Date07 28 2022 Product Code Qon 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 P080025S266 MEDTRONIC NEUROMODULATION7000 Central Avenue Nems Rcw225minneapolis, MN 55432 PMA NumberP080025 Supplement NumberS266 Date Received07/20/2022 Decision Date07/28/2022 Product Code QON  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 (SNS Bowel)	2022-07-28