Medtronic Inc 8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp930039 Supplement Numbers248 Date Received01 09 2023 Decision Date01 16 2023 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 Numbers248 Date Received01 09 2023 Decision Date01 16 2023 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
Medtronic, Inc.8200 Coral Sea Street N.e.mounds View, MN 55112 PMA NumberP930039 Supplement NumberS248 Date Received01/09/2023 Decision Date01/16/2023 Product Code NVN  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
CapSureFix Novus Lead2023-01-16

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