Medtronic Vascular Inc3033 Campus Driveplymouth Mn 55441 Pma Numberp060001 Supplement Numbers035 Date Received11 15 2022 Decision Date12 15 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 Numbers035 Date Received11 15 2022 Decision Date12 15 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 Filings

Device Company	Device	Date
PMA P060001S035 MEDTRONIC VASCULAR INC3033 Campus Driveplymouth, MN 55441 PMA NumberP060001 Supplement NumberS035 Date Received11/15/2022 Decision Date12/15/2022 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 System, Protégé RX Carotid Stent System	2022-12-15