This page includes the latest FDA filings for Cordis Us Corporation14201 N W 60th Avenuemiami Lakes Fl 33014 Pma Numberp020036 Supplement Numbers048 Date Received11 21 2022 Decision Date12 16 2022 Product Code Nio 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.
Device Company | Device | Date |
|---|---|---|
| Cordis US Corporation14201 N.w. 60th Avenuemiami Lakes, FL 33014 PMA NumberP020036 Supplement NumberS048 Date Received11/21/2022 Decision Date12/16/2022 Product Code NIO Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No | Cordis® S.M.A.R.T.® CONTROL® Nitinol Stent Systems, Cordis® S.M.A.R.T.® and S.M.A.R.T.® CONTROL® Vascular Stent Systems, | 2022-12-16 |