Medtronic Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp860004 Supplement Numbers389 Date Received04 08 2022 Decision Date05 05 2022 Product Code Lkk Advisory Committee General Hospital 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 Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp860004 Supplement Numbers389 Date Received04 08 2022 Decision Date05 05 2022 Product Code Lkk Advisory Committee General Hospital 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 P860004S389 MEDTRONIC Inc.7000 Central Avenue Neminneapolis, MN 55432-3576 PMA NumberP860004 Supplement NumberS389 Date Received04/08/2022 Decision Date05/05/2022 Product Code LKK  Advisory Committee General Hospital Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	SynchroMed® Infusion System, Ascenda® Intrathecal Catheters	2022-05-05