This page includes the latest FDA filings for Cvrx Inc 9201 West Broadway Ave Ste 650minneapolis Mn 55445 Pma Numberp180050 Supplement Numbers002 Date Received09 20 2021 Decision Date04 14 2022 Product Code Dsr Advisory Committee Cardiovascular Supplement Typenormal 180 Day Track Supplement Reason Change Design Components Specifications Material 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 |
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CVRx, INC.9201 West Broadway Ave, Ste 650minneapolis, MN 55445 PMA NumberP180050 Supplement NumberS002 Date Received09/20/2021 Decision Date04/14/2022 Product Code DSR Advisory Committee Cardiovascular Supplement Typenormal 180 Day Track Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No | Barostimâ„¢ System | 2022-04-14 |