Astron Pulsar Stent System and Pulsar-18 Stent System
FDA premarket approval P160025/S009 · decided 2019-12-04
Approval details
- PMA number
- P160025
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Astron Pulsar Stent System and Pulsar-18 Stent System
- Generic name
- STENT, SUPERFICIAL FEMORAL ARTERY
- Applicant
- Biotronik AG
- Date received
- 2019-11-04
- Decision date
- 2019-12-04
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- NIP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bülach
- Statement
- Modifications to routine bioburden and endotoxin monitoring.
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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 |