VIGOR DDD PACEMAKER SYSTEM
FDA premarket approval P840068/S021 · decided 1994-10-21
Approval details
- PMA number
- P840068
- Supplement
- S021
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- VIGOR DDD PACEMAKER SYSTEM
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 1993-07-13
- Decision date
- 1994-10-21
- Days to decision
- 465 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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