PARADYM VR/DR
FDA premarket approval P980049/S065 · decided 2012-04-10
Approval details
- PMA number
- P980049
- Supplement
- S065
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- PARADYM VR/DR
- Generic name
- DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2011-09-01
- Decision date
- 2012-04-10
- Days to decision
- 222 days
- Decision code
- APPR
- Product code
- MRM
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- APPROVAL FOR THE PARADYM RF CRT-D AND PARADYM RF ICD.
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