Abbott Vascular Devices3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp050007 Supplement Numbers042 Date Received11 16 2022 Decision Date12 16 2022 Product Code Mgb 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 Devices3200 Lakeside Drivesanta Clara Ca 95054 Pma Numberp050007 Supplement Numbers042 Date Received11 16 2022 Decision Date12 16 2022 Product Code Mgb 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 P050007S042 ABBOTT VASCULAR DEVICES3200 Lakeside Drivesanta Clara, CA 95054 PMA NumberP050007 Supplement NumberS042 Date Received11/16/2022 Decision Date12/16/2022 Product Code MGB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	StarClose SE Vascular Closure System	2022-12-16