Abbott Vascular Idef Technologies Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp120020 Supplement Numbers028 Date Received09 30 2022 Decision Date11 22 2022 Product Code Nip Advisory Committee Cardiovascular Supplement Typereal Time Process Supplement Reason Change Design Components Specifications Material Expedited Review Granted No

FDA Filings

This page includes the latest FDA filings for Abbott Vascular Idef Technologies Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp120020 Supplement Numbers028 Date Received09 30 2022 Decision Date11 22 2022 Product Code Nip Advisory Committee Cardiovascular Supplement Typereal Time Process 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.

FDA Registration(s)

FDA Filings

Device
Company
DeviceDate
ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP120020 Supplement NumberS028 Date Received09/30/2022 Decision Date11/22/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Typereal-time Process Supplement Reason Change Design/components/specifications/material Expedited Review Granted? No
 Supera Peripheral Stent System2022-11-22

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