Astron Pulsar and Pulsar-18 Stent Systems
FDA premarket approval P160025/S005 · decided 2018-08-22
Approval details
- PMA number
- P160025
- Supplement
- S005
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Labeling Change - PAS
- Trade name
- Astron Pulsar and Pulsar-18 Stent Systems
- Generic name
- STENT, SUPERFICIAL FEMORAL ARTERY
- Applicant
- Biotronik AG
- Date received
- 2018-06-21
- Decision date
- 2018-08-22
- Days to decision
- 62 days
- Decision code
- APPR
- Product code
- NIP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bülach
- Statement
- Approval for updated labeling to include clinical data from the BIOFLEX-I Study.
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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 |