VENTAK AV FOR ASTRID
FDA premarket approval P960040/S019 · decided 2001-01-23
Approval details
- PMA number
- P960040
- Supplement
- S019
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- VENTAK AV FOR ASTRID
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 2000-12-01
- Decision date
- 2001-01-23
- Days to decision
- 53 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL FOR MODIFICATIONS TO THE MODEL 6942 BI-DIRECTIONAL TORQUE WRENCH.
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