Medtronic Vascular Inc3033 Campus Driveplymouth Mn 55441 Pma Numberp110023 Supplement Numbers036 Date Received11 15 2022 Decision Date12 15 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 Numbers036 Date Received11 15 2022 Decision Date12 15 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 P110023S036 MEDTRONIC VASCULAR INC3033 Campus Driveplymouth, MN 55441 PMA NumberP110023 Supplement NumberS036 Date Received11/15/2022 Decision Date12/15/2022 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 with Entrust™ Delivery Syste	2022-12-15