STIMPOD NMS460 Nerve Stimulator— 510(k) K252712

Name: FDA 510(k) clearance K252712
Creator: U.S. Food and Drug Administration
Published: 2026-05-28

Substantially Equivalent

Algiamed Technologies USA, Inc.

FDA 510(k) clearance K252712 for STIMPOD NMS460 Nerve Stimulator, Substantially Equivalent on 2026-05-28. Applicant: Algiamed Technologies USA, Inc.. Device class: 2.

Clearance details

Applicant: Algiamed Technologies USA, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-08-27
Decision date: 2026-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Mary, FL, US

Download summary PDF View on FDA.gov ↗

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