Medtronic Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp990034 Supplement Numbers042 Date Received07 22 2022 Decision Date08 19 2022 Product Code Lkk Advisory Committee General Hospital Supplement Typespecial Immediate Track Supplement Reason Labeling Change Indications Instructions Shelf Life Tradename Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Medtronic Inc 7000 Central Avenue Neminneapolis Mn 55432 3576 Pma Numberp990034 Supplement Numbers042 Date Received07 22 2022 Decision Date08 19 2022 Product Code Lkk Advisory Committee General Hospital Supplement Typespecial Immediate Track Supplement Reason Labeling Change Indications Instructions Shelf Life Tradename 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 P990034S042 MEDTRONIC Inc.7000 Central Avenue Neminneapolis, MN 55432-3576 PMA NumberP990034 Supplement NumberS042 Date Received07/22/2022 Decision Date08/19/2022 Product Code LKK  Advisory Committee General Hospital Supplement Typespecial (immediate Track) Supplement Reason Labeling Change - Indications/instructions/shelf Life/tradename Expedited Review Granted? No	IsoMed Infusion System	2022-08-19