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 | 5086 MRI CAPSUREFIX MRI SURESCAN LEADS |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | Medtronic, Inc 8200 Coral Sea Street NE Mounds View, MN 55112 |
PMA Number | P090013 |
Supplement Number | S200 |
Date Received | 03/16/2015 |
Decision Date | 09/11/2015 |
Product Codes |
LWP NVN |
Advisory Committee |
Cardiovascular |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Review Memo | Review Memo |
Approval Order Statement APPROVAL OF THE EVERA MRI XT/S DR AND VR IMPLANTABLE CARDIOVERTERDEFIBRILLATOR DEVICES AND PROGRAMMER APPLICATION SOFTWARE MODEL SW033 AS WELL AS EXTENSION OF MR CONDITIONAL LABELING AND USE FOR SPRINT QUATTRO SECURE LEAD MODELS 6935M AND 6947M AS MRI SURESCAN LABELED 55 AND 62CM LEADS. IN ADDITION TO THE SYSTEM COMPONENTS LISTED, THE USE OF THE CAPSUREFIX MRI SURESCAN LEAD MODEL 5086MRI AND CAPSUREFIX NOVUS MRI SURESCAN LEAD MODEL 5076 WITH THE EVERA MRI DR (DUAL CHAMBER)SYSTEM WHEN AN ATRIAL PACE/SENSE LEAD IS INDICATED. FURTHERMORE, YOU REQUESTED APPROVAL TO USE CARELINK MONITOR MODEL 2490C, CARELINK EXPRESS MONITOR 2020B, CARDIOSIGHT READER MODEL2020A, MYCARELINK MONITOR MODEL 24950 AND DEVICE DATA MANAGEMENT APPLICATION (DDMA) MODEL 2491 TO PROVIDE PATIENT AND DEVICE DATA TRANSFER FROM THE EVERA MRI DEVICES. |
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