Vecttor VT-300— 510(k) K231575

Substantially Equivalent

Artaflex, Inc.

FDA 510(k) clearance K231575 for Vecttor VT-300, Substantially Equivalent on 2024-02-08. Applicant: Artaflex, Inc.. Device class: 2.

Clearance details

Applicant: Artaflex, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2023-05-31
Decision date: 2024-02-08
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Markham, CA

Download summary PDF View on FDA.gov ↗

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