Minerva Surgical Inc 4255 Burton Drivesanta Clara Ca 95054 Pma Numberp000040 Supplement Numbers042 Date Received04 27 2022 Decision Date05 26 2022 Product Code Mnb Advisory Committee Obstetrics Gynecology Supplement Typenormal 180 Day Track No User Fee Supplement Reason Location Change Manufacturer Sterilizer Packager Supplier Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Minerva Surgical Inc 4255 Burton Drivesanta Clara Ca 95054 Pma Numberp000040 Supplement Numbers042 Date Received04 27 2022 Decision Date05 26 2022 Product Code Mnb Advisory Committee Obstetrics Gynecology Supplement Typenormal 180 Day Track No User Fee Supplement Reason Location 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
Minerva Surgical, Inc.4255 Burton Drivesanta Clara, CA 95054 PMA NumberP000040 Supplement NumberS042 Date Received04/27/2022 Decision Date05/26/2022 Product Code MNB  Advisory Committee Obstetrics/Gynecology Supplement Typenormal 180 Day Track No User Fee Supplement Reason Location Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Genesys HTA System2022-05-26

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