VENTAK(R) MODEL 1555 PULSE GENERATOR
FDA premarket approval P830060/S020 · decided 1990-09-17
Approval details
- PMA number
- P830060
- Supplement
- S020
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- VENTAK(R) MODEL 1555 PULSE GENERATOR
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 1990-07-23
- Decision date
- 1990-09-17
- Days to decision
- 56 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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