Abbott Vascular Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp040038 Supplement Numbers041 Date Received11 21 2022 Decision Date01 31 2023 Product Code Nim 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 Inc 3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp040038 Supplement Numbers041 Date Received11 21 2022 Decision Date01 31 2023 Product Code Nim 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 P040038S041 ABBOTT VASCULAR INC.3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP040038 Supplement NumberS041 Date Received11/21/2022 Decision Date01/31/2023 Product Code NIM  Advisory Committee Cardiovascular Supplement Type135 Review Track For 30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	XACT Carotid Stent System	2023-01-31