Abbott Vascular Inc 26531 Ynez Roadtemecula Ca 92591 Pma Numberp970020 Supplement Numbers086 Date Received08 09 2022 Decision Date09 07 2022 Product Code Maf 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 Vascular Inc 26531 Ynez Roadtemecula Ca 92591 Pma Numberp970020 Supplement Numbers086 Date Received08 09 2022 Decision Date09 07 2022 Product Code Maf 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 P970020S086 ABBOTT VASCULAR INC.26531 Ynez Roadtemecula, CA 92591 PMA NumberP970020 Supplement NumberS086 Date Received08/09/2022 Decision Date09/07/2022 Product Code MAF  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	MULTI-LINK RX ULTRA™ Coronary Stent System	2022-09-07