DeviceClearance

SINEXUS SINUS STENT GEN 2, MODEL 1999-25— 510(k) K092401

Substantially Equivalent

Sinexus, Inc.

FDA 510(k) clearance K092401 for SINEXUS SINUS STENT GEN 2, MODEL 1999-25, Substantially Equivalent on 2009-11-17. Applicant: Sinexus, Inc..

Clearance details

Applicant
Sinexus, Inc.
Product code
Code LYA
Advisory panel
Ear, Nose, Throat
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Palo Alto, CA, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.