Medtronic Inc 710 Medtronic Parkwayminneapolis Mn 55432 Pma Numberp130021 Supplement Numbers122 Date Received09 12 2022 Decision Date09 27 2022 Product Code Npt 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 710 Medtronic Parkwayminneapolis Mn 55432 Pma Numberp130021 Supplement Numbers122 Date Received09 12 2022 Decision Date09 27 2022 Product Code Npt 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.710 Medtronic Parkwayminneapolis,, MN 55432 PMA NumberP130021 Supplement NumberS122 Date Received09/12/2022 Decision Date09/27/2022 Product Code NPT  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
 EnVeo R Delivery Catheter System, EnVeo PRO Delivery Catheter System, Evolut PRO+ Delivery Catheter System2022-09-27

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