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PMA de la FDA

Estimulador, nervio autónomo, implantado para la rehabilitación del accidente cerebrovascular

Número de PMA: P210007 · 2026-09-16

SolicitanteMobia Medical, Inc.
Fecha de decisión2026-09-16
Número PMAP210007
Código de productoQPY
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorPM

Resumen del dispositivo

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.

Preguntas frecuentes

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.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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