Reliance 4-Front, 4-Site IS-1 Defibrillation
FDA premarket approval P910073/S153 · decided 2019-02-28
Approval details
- PMA number
- P910073
- Supplement
- S153
- Supplement type
- Real-Time Process
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- Reliance 4-Front, 4-Site IS-1 Defibrillation
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2018-12-26
- Decision date
- 2019-02-28
- Days to decision
- 64 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Approval for sales packaging and label changes.
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