IMPLANTABLE CARDIVERTER DEFIBRILLATORS
FDA premarket approval P980016/S620 · decided 2017-07-18
Approval details
- PMA number
- P980016
- Supplement
- S620
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- IMPLANTABLE CARDIVERTER DEFIBRILLATORS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Medtronic Cardiac Rhythm Disease Management
- Date received
- 2017-01-31
- Decision date
- 2017-07-18
- Days to decision
- 168 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Mounds View, MN
- Statement
- Approval for a change to a 11-pin feedthrough design and associated design and manufacturing changes for ICD and CRT-D devices.
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