Medtronic Cryocath Lp8200 Coral Sea Streetms Mvs46mounds View Mn 55112 Pma Numberp100010 Supplement Numbers129 Date Received07 25 2022 Decision Date08 24 2022 Product Code Oae 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 Medtronic Cryocath Lp8200 Coral Sea Streetms Mvs46mounds View Mn 55112 Pma Numberp100010 Supplement Numbers129 Date Received07 25 2022 Decision Date08 24 2022 Product Code Oae 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 P100010S129 Medtronic CryoCath LP8200 Coral Sea Streetms Mvs46mounds View, MN 55112 PMA NumberP100010 Supplement NumberS129 Date Received07/25/2022 Decision Date08/24/2022 Product Code OAE  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Artic Front Advance Cardiac Cryoablation Catheter, Arctic Front Advance Pro Cardiac Cryoablation Catheter	2022-08-24