Medtronic Inc 8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp930039 Supplement Numbers243 Date Received05 20 2022 Decision Date06 01 2022 Product Code Nvn 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 Numberp930039 Supplement Numbers243 Date Received05 20 2022 Decision Date06 01 2022 Product Code Nvn 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 P930039S243 Medtronic, Inc.8200 Coral Sea Street N.e.mounds View, MN 55112 PMA NumberP930039 Supplement NumberS243 Date Received05/20/2022 Decision Date06/01/2022 Product Code NVN  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	CapSureFix Lead, CapSureFix Novus Lead, Vitatron Crystalline Active Fixation Lead	2022-06-01