Pulsar-18 T3
FDA premarket approval P160025/S019 · decided 2025-03-03
Approval details
- PMA number
- P160025
- Supplement
- S019
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Pulsar-18 T3
- Generic name
- STENT, SUPERFICIAL FEMORAL ARTERY
- Applicant
- Biotronik AG
- Date received
- 2024-12-18
- Decision date
- 2025-03-03
- Days to decision
- 75 days
- Decision code
- APPR
- Product code
- NIP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bülach
- Statement
- Approval for dimensional modifications to the Luer lock connectors and manifolds as well as the corresponding injection molding equipment
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| PHERON PERIPHERAL PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER (K052757) | Biotronik AG | 2005-10-28 |