Medtronic Vascular Inc3033 Campus Driveplymouth Mn 55441 Pma Numberp060001 Supplement Numbers034 Date Received05 25 2022 Decision Date06 03 2022 Product Code Nim 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 Vascular Inc3033 Campus Driveplymouth Mn 55441 Pma Numberp060001 Supplement Numbers034 Date Received05 25 2022 Decision Date06 03 2022 Product Code Nim 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 VASCULAR INC3033 Campus Driveplymouth, MN 55441 PMA NumberP060001 Supplement NumberS034 Date Received05/25/2022 Decision Date06/03/2022 Product Code NIM  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Protégé GPS Self Expanding Peripheral Stent System2022-06-03

Related Finance Registrations

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