Medtronic Vascular Inc3033 Campus Driveplymouth Mn 55441 Pma Numberp110023 Supplement Numbers035 Date Received05 25 2022 Decision Date06 03 2022 Product Code Nip 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 Numberp110023 Supplement Numbers035 Date Received05 25 2022 Decision Date06 03 2022 Product Code Nip 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 P110023S035 MEDTRONIC VASCULAR INC3033 Campus Driveplymouth, MN 55441 PMA NumberP110023 Supplement NumberS035 Date Received05/25/2022 Decision Date06/03/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	EverFlex Self-Expanding Peripheral Stent System, EverFlex Self-Expanding Peripheral Stent System with Entrust Delivery S	2022-06-03