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FDA PMA

Vagus nerve stimulator for rheumatoid arthritis

PMA Number: P240039 · 2026-02-18

ApplicantSetPoint Medical
Decision Date2026-02-18
PMA NumberP240039
Product CodeSFJ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeNE

Device Summary

Vagus nerve stimulator for rheumatoid arthritis is the device name listed in this FDA 510(k) record. The listed applicant is SetPoint Medical. It received FDA 510(k) clearance on 2026-02-18. The device is classified under product code SFJ. It was reviewed by the NE advisory panel.

Frequently Asked Questions

What is the Vagus nerve stimulator for rheumatoid arthritis?

Vagus nerve stimulator for rheumatoid arthritis is a medical device that received FDA 510(k) clearance on 2026-02-18. The listed applicant is SetPoint Medical.

When did Vagus nerve stimulator for rheumatoid arthritis receive FDA 510(k) clearance?

The clearance date for Vagus nerve stimulator for rheumatoid arthritis can be found in the official FDA records.

Who is the listed applicant for Vagus nerve stimulator for rheumatoid arthritis?

The FDA 510(k) record lists SetPoint Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vagus nerve stimulator for rheumatoid arthritis?

The FDA product code for Vagus nerve stimulator for rheumatoid arthritis is SFJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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