Amplia MRI, Amplia MRI Quad, Brava, Brava Quad, Claria MRI, Claria Quad, Compia MRI, Compia MRI Quad, Viva Quad S, Viva
FDA premarket approval P010031/S585 · decided 2017-03-13
Approval details
- PMA number
- P010031
- Supplement
- S585
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Amplia MRI, Amplia MRI Quad, Brava, Brava Quad, Claria MRI, Claria Quad, Compia MRI, Compia MRI Quad, Viva Quad S, Viva
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2017-02-17
- Decision date
- 2017-03-13
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Updated test equipment for use in battery manufacturing.
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