Medtronic Inc 8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp890003 Supplement Numbers452 Date Received04 14 2022 Decision Date04 21 2022 Product Code Nvz Advisory Committee Cardiovascular 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 8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp890003 Supplement Numbers452 Date Received04 14 2022 Decision Date04 21 2022 Product Code Nvz Advisory Committee Cardiovascular 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 P890003S452 Medtronic, Inc.8200 Coral Sea Street N.e.mounds View, MN 55112 PMA NumberP890003 Supplement NumberS452 Date Received04/14/2022 Decision Date04/21/2022 Product Code NVZ  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	CapSure VDD-2 Lead, Service Kit-Pacemaker Repair Kit, Vitatron Brilliant S+ VDD Lead	2022-04-21