Medtronic Cryocath Lp8200 Coral Sea Streetms Mvs46mounds View Mn 55112 Pma Numberp100010 Supplement Numbers134 Date Received12 21 2022 Decision Date01 19 2023 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 Numbers134 Date Received12 21 2022 Decision Date01 19 2023 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 P100010S134 Medtronic CryoCath LP8200 Coral Sea Streetms Mvs46mounds View, MN 55112 PMA NumberP100010 Supplement NumberS134 Date Received12/21/2022 Decision Date01/19/2023 Product Code OAE  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No	Arctic Front Advance® Cardiac CryoAblation Catheters	2023-01-19