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FDA PMA

Stimulator, autonomic nerve, implanted for stroke rehabilitation

PMA Number: P210007 · 2026-09-16

Decision Date2026-09-16
PMA NumberP210007
Product CodeQPY
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteePM

Device Summary

Stimulator, autonomic nerve, implanted for stroke rehabilitation is the device name listed in this FDA 510(k) record. The listed applicant is Mobia Medical, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code QPY. It was reviewed by the PM advisory panel.

Frequently Asked Questions

What is the Stimulator, autonomic nerve, implanted for stroke rehabilitation?

Stimulator, autonomic nerve, implanted for stroke rehabilitation is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Mobia Medical, Inc..

When did Stimulator, autonomic nerve, implanted for stroke rehabilitation receive FDA 510(k) clearance?

The clearance date for Stimulator, autonomic nerve, implanted for stroke rehabilitation can be found in the official FDA records.

Who is the listed applicant for Stimulator, autonomic nerve, implanted for stroke rehabilitation?

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

What is the FDA product code for Stimulator, autonomic nerve, implanted for stroke rehabilitation?

The FDA product code for Stimulator, autonomic nerve, implanted for stroke rehabilitation is QPY.

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.

Official Source

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

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