Cvrx Inc 9201 West Broadway Ave Ste 650minneapolis Mn 55445 Pma Numberp180050 Supplement Numbers005 Date Received03 28 2022 Decision Date04 26 2022 Product Code Dsr 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 Cvrx Inc 9201 West Broadway Ave Ste 650minneapolis Mn 55445 Pma Numberp180050 Supplement Numbers005 Date Received03 28 2022 Decision Date04 26 2022 Product Code Dsr 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 P180050S005 CVRx, INC.9201 West Broadway Ave, Ste 650minneapolis, MN 55445 PMA NumberP180050 Supplement NumberS005 Date Received03/28/2022 Decision Date04/26/2022 Product Code DSR  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Barostim System	2022-04-26