Abbott Vascularp O Box 9018temecula Ca 92589 9018 Pma Numberp020047 Supplement Numbers075 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 Vascularp O Box 9018temecula Ca 92589 9018 Pma Numberp020047 Supplement Numbers075 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 P020047S075 ABBOTT VASCULARp.o. Box 9018temecula, CA 92589-9018 PMA NumberP020047 Supplement NumberS075 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 VISION™ RX Coronary Stent System, MULTI-LINK VISION™ RX 2.75 mm Coronary Stent System, MULTI-LINK MINI VISION	2022-09-07