SINEXUS SINUS STENT GEN 2, MODEL 1999-25— 510(k) K092401
Substantially EquivalentSinexus, Inc.
FDA 510(k) clearance K092401 for SINEXUS SINUS STENT GEN 2, MODEL 1999-25, Substantially Equivalent on 2009-11-17. Applicant: Sinexus, Inc.. Device class: 1.
Clearance details
- Applicant
- Sinexus, Inc.
- Product code
- Code LYA
- Device class
- Class 1
- Regulation
- 21 CFR 874.4780
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Palo Alto, CA, US
Recent devices under product code LYA
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