St Jude Medical14900 Minnetonka Ind Rdminnetonka Mn 55345 Pma Numberp960016 Supplement Numbers089 Date Received11 14 2022 Decision Date12 08 2022 Product Code Lpb 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 St Jude Medical14900 Minnetonka Ind Rdminnetonka Mn 55345 Pma Numberp960016 Supplement Numbers089 Date Received11 14 2022 Decision Date12 08 2022 Product Code Lpb 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 P960016S089 St. Jude Medical14900 Minnetonka Ind Rdminnetonka, MN 55345 PMA NumberP960016 Supplement NumberS089 Date Received11/14/2022 Decision Date12/08/2022 Product Code LPB  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Livewire TC Ablation Catheter	2022-12-08