Ingevity + Lead - Active Fixation
FDA premarket approval P150012/S083 · decided 2019-12-16
Approval details
- PMA number
- P150012
- Supplement
- S083
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Ingevity + Lead - Active Fixation
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2019-09-26
- Decision date
- 2019-12-16
- Days to decision
- 81 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- Approval to add the INGEVITY+ (plus) leads to the INGEVITY MRI lead family.
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