Medtronic Inc8200 Coral Sea Street Nemounds View Mn 55112 Pma Numberp090013 Supplement Numbers322 Date Received05 20 2022 Decision Date06 01 2022 Product Codes Nvn Lwp 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 Inc8200 Coral Sea Street Nemounds View Mn 55112 Pma Numberp090013 Supplement Numbers322 Date Received05 20 2022 Decision Date06 01 2022 Product Codes Nvn Lwp 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
Medtronic, Inc8200 Coral Sea Street Nemounds View, MN 55112 PMA NumberP090013 Supplement NumberS322 Date Received05/20/2022 Decision Date06/01/2022 Product Codes NVN LWP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
CapSureFix MRI Lead2022-06-01

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