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PMA de la FDA

Estimulador, neuromuscular, músculos lumbares inferiores, implantado completamente para el alivio del dolor

Número de PMA: P190021 · 2025-06-20

SolicitanteMainstay Medical Limited
Fecha de decisión2025-06-20
Número PMAP190021
Código de productoQLK
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorNE

Resumen del dispositivo

Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Mainstay Medical Limited. It received FDA 510(k) clearance on 2025-06-20. The device is classified under product code QLK. It was reviewed by the NE advisory panel.

Preguntas frecuentes

What is the Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief?

Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2025-06-20. The listed applicant is Mainstay Medical Limited.

When did Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief receive FDA 510(k) clearance?

The clearance date for Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief can be found in the official FDA records.

Who is the listed applicant for Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief?

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

What is the FDA product code for Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief?

The FDA product code for Stimulator, neuromuscular, lower back muscles, totally implanted for pain relief is QLK.

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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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