Cordis Us Corporation14201 N W 60th Avenuemiami Lakes Fl 33014 Pma Numberp030047 Supplement Numbers044 Date Received04 18 2022 Decision Date04 27 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 Cordis Us Corporation14201 N W 60th Avenuemiami Lakes Fl 33014 Pma Numberp030047 Supplement Numbers044 Date Received04 18 2022 Decision Date04 27 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 P030047S044 Cordis US Corporation14201 N.w. 60th Avenuemiami Lakes, FL 33014 PMA NumberP030047 Supplement NumberS044 Date Received04/18/2022 Decision Date04/27/2022 Product Code NIM  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Cordis PRECISE Nitinol Stent System	2022-04-27