AMStent® Tracheobronchial Covered Stent System— 510(k) DEN230087

Name: FDA 510(k) clearance DEN230087
Creator: U.S. Food and Drug Administration
Published: 2024-10-16

Unknown

Peytant Solutions, Inc.

FDA 510(k) clearance DEN230087 for AMStent® Tracheobronchial Covered Stent System, Unknown on 2024-10-16. Applicant: Peytant Solutions, Inc.. Device class: 2.

Clearance details

Applicant: Peytant Solutions, Inc.
Product code: Code SDB
Device class: Class 2
Regulation: 21 CFR 868.3721
Advisory panel: Anesthesiology
Date received: 2023-12-20
Decision date: 2024-10-16
Decision: Unknown
Clearance type: Direct
Location: Plymouth, MN, US

View on FDA.gov ↗

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