Medtronic Vascular3576 Unocal Placesanta Rosa Ca 95403 Pma Numberp100021 Supplement Numbers101 Date Received01 25 2022 Decision Date02 24 2022 Product Code Mih 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 Vascular3576 Unocal Placesanta Rosa Ca 95403 Pma Numberp100021 Supplement Numbers101 Date Received01 25 2022 Decision Date02 24 2022 Product Code Mih 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 Vascular3576 Unocal Placesanta Rosa, CA 95403 PMA NumberP100021 Supplement NumberS101 Date Received01/25/2022 Decision Date02/24/2022 Product Code MIH  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Endurant Stent Graft System, Endurant II Stent Graft System, Endurant IIS Stent Graft System2022-02-24

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