AMPLIA MRI, AMPLIA MRI QUAD, BRAVA, BRAVA QUAD, COMPIA MRI,COMPIA MRI QUAD, VIVA QUAD S, VIVA QUAD XT, VIVA S, VIVA XT C
FDA premarket approval P010031/S547 · decided 2016-06-16
Approval details
- PMA number
- P010031
- Supplement
- S547
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- AMPLIA MRI, AMPLIA MRI QUAD, BRAVA, BRAVA QUAD, COMPIA MRI,COMPIA MRI QUAD, VIVA QUAD S, VIVA QUAD XT, VIVA S, VIVA XT C
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2016-04-28
- Decision date
- 2016-06-16
- Days to decision
- 49 days
- Decision code
- APPR
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Approval for modifications to the Telemetry M Module.
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