Abbott Vascular3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp110019 Supplement Numbers121 Date Received05 23 2022 Decision Date06 22 2022 Product Code Niq 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 Abbott Vascular3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp110019 Supplement Numbers121 Date Received05 23 2022 Decision Date06 22 2022 Product Code Niq 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 P110019S121 ABBOTT VASCULAR3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP110019 Supplement NumberS121 Date Received05/23/2022 Decision Date06/22/2022 Product Code NIQ  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	XIENCE Skypoint Everolimus Eluting Coronary Stent System	2022-06-22