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PMA de la FDA

Stimulator, spinal-cord, totally implanted for pain relief

Número de PMA: P130028 · 2020-05-05

SolicitanteNuvectra Corporation
Fecha de decisión2020-05-05
Número PMAP130028
Código de productoLGW
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorNE

Resumen del dispositivo

Stimulator, spinal-cord, totally implanted for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Nuvectra Corporation. It received FDA 510(k) clearance on 2020-05-05. The device is classified under product code LGW. It was reviewed by the NE advisory panel.

Preguntas frecuentes

What is the Stimulator, spinal-cord, totally implanted for pain relief?

Stimulator, spinal-cord, totally implanted for pain relief is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Nuvectra Corporation.

When did Stimulator, spinal-cord, totally implanted for pain relief receive FDA 510(k) clearance?

The clearance date for Stimulator, spinal-cord, totally implanted for pain relief can be found in the official FDA records.

Who is the listed applicant for Stimulator, spinal-cord, totally implanted for pain relief?

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

What is the FDA product code for Stimulator, spinal-cord, totally implanted for pain relief?

The FDA product code for Stimulator, spinal-cord, totally implanted for pain relief is LGW.

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Fuente oficial

Ver en la base de datos de la FDA →

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