Abbott Vascular Idef Technologies Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp120020 Supplement Numbers030 Date Received11 21 2022 Decision Date01 31 2023 Product Code Nip Advisory Committee Cardiovascular Supplement Type135 Review Track For 30 Day Notice Supplement Reason Process Change Manufacturer Sterilizer Packager Supplier 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 Numbers030 Date Received11 21 2022 Decision Date01 31 2023 Product Code Nip Advisory Committee Cardiovascular Supplement Type135 Review Track For 30 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 P120020S030 ABBOTT VASCULAR (IDEF TECHNOLOGIES INC)3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP120020 Supplement NumberS030 Date Received11/21/2022 Decision Date01/31/2023 Product Code NIP  Advisory Committee Cardiovascular Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Supera Peripheral Stent System	2023-01-31