Medtronic Cardiac Rhythm Disease Management8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp010031 Supplement Numbers800 Date Received08 23 2022 Decision Date08 25 2022 Product Code Nik 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 Cardiac Rhythm Disease Management8200 Coral Sea Street N E Mounds View Mn 55112 Pma Numberp010031 Supplement Numbers800 Date Received08 23 2022 Decision Date08 25 2022 Product Code Nik 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 Registration(s)

FDA Filings

Device
Company
DeviceDate
MEDTRONIC CARDIAC RHYTHM DISEASE MANAGEMENT8200 Coral Sea Street N.e.mounds View, MN 55112 PMA NumberP010031 Supplement NumberS800 Date Received08/23/2022 Decision Date08/25/2022 Product Code NIK  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D, Compia2022-08-25

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