Medtronic Irelandparkmore Business Park Westgalway Pma Numberp030009 Supplement Numbers107 Date Received03 23 2022 Decision Date04 19 2022 Product Code Maf 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 Irelandparkmore Business Park Westgalway Pma Numberp030009 Supplement Numbers107 Date Received03 23 2022 Decision Date04 19 2022 Product Code Maf 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 IRELANDparkmore Business Park Westgalway  PMA NumberP030009 Supplement NumberS107 Date Received03/23/2022 Decision Date04/19/2022 Product Code MAF  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
 Integrity Rapid Exchange Coronary Stent System, Integrity Over The Wire Coronary Stent System2022-04-19

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