Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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Device | Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Eve |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | Medtronic, Inc. 8200 Coral Sea Street NE MV MVS11 Mounds View, MN 55112 |
PMA Number | P220012 |
Supplement Number | S017 |
Date Received | 03/05/2024 |
Decision Date | 04/04/2024 |
Product Codes |
LWS NVY |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement implementation of a central resin dryer conveyance system for use in battery manufacturing at Medtronic Energy and Component Center |
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