Foot Drop System (Model XFT-2001D)— 510(k) K162718

Name: FDA 510(k) clearance K162718
Creator: U.S. Food and Drug Administration
Published: 2017-11-30

Substantially Equivalent

Shenzhen Xft Medical Limited

FDA 510(k) clearance K162718 for Foot Drop System (Model XFT-2001D), Substantially Equivalent on 2017-11-30. Applicant: Shenzhen Xft Medical Limited. Device class: 2.

Clearance details

Applicant: Shenzhen Xft Medical Limited
Product code: Code GZI
Device class: Class 2
Regulation: 21 CFR 882.5810
Advisory panel: Neurology
Date received: 2016-09-29
Decision date: 2017-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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