AXIOS Stent with Electrocautery Enhanced Delivery System
FDA 510(k) clearance K150692 · decided 2015-08-05
Clearance details
- K-number
- K150692
- Device name
- AXIOS Stent with Electrocautery Enhanced Delivery System
- Applicant
- Boston Scientific Corp
- Decision
- Substantially Equivalent
- Date received
- 2015-03-18
- Decision date
- 2015-08-05
- Days to decision
- 140 days
- Clearance type
- Traditional
- Product code
- PCU
- Device class
- 2
- Regulation number
- 876.5015
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mountain View, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.