Abbott Vascular Inc 400 Saginaw Driveredwood City Ca 94063 Pma Numberp960043 Supplement Numbers119 Date Received11 16 2022 Decision Date12 16 2022 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 400 Saginaw Driveredwood City Ca 94063 Pma Numberp960043 Supplement Numbers119 Date Received11 16 2022 Decision Date12 16 2022 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 P960043S119 ABBOTT VASCULAR INC.400 Saginaw Driveredwood City, CA 94063 PMA NumberP960043 Supplement NumberS119 Date Received11/16/2022 Decision Date12/16/2022 Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Prostar™ XL Percutaneous Vascular Surgical System, Perclose ProGlide™ Suture-Mediated Closure System, Perclose™ ProStyle	2022-12-16