Medtronic Inc 8200 Coral Sea Street Nems Mv S11mounds View Mn 55112 Pma Numberp980035 Supplement Numbers737 Date Received01 09 2023 Decision Date01 16 2023 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 Nems Mv S11mounds View Mn 55112 Pma Numberp980035 Supplement Numbers737 Date Received01 09 2023 Decision Date01 16 2023 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
MEDTRONIC Inc.8200 Coral Sea Street Nems Mv S11mounds View, MN 55112 PMA NumberP980035 Supplement NumberS737 Date Received01/09/2023 Decision Date01/16/2023 Product Code NVZ  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Adapta, Versa, Sensia IPG, Advisa SR MRI IPG, Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR M2023-01-16

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.