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PMA de la FDA

Stimulator, bone growth, non-invasive

Número de PMA: P910066 · 2020-01-23

SolicitanteDjo, LLC
Fecha de decisión2020-01-23
Número PMAP910066
Código de productoLOF
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Djo, LLC. It received FDA 510(k) clearance on 2020-01-23. The device is classified under product code LOF. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Stimulator, bone growth, non-invasive?

Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2020-01-23. The listed applicant is Djo, LLC.

When did Stimulator, bone growth, non-invasive receive FDA 510(k) clearance?

The clearance date for Stimulator, bone growth, non-invasive can be found in the official FDA records.

Who is the listed applicant for Stimulator, bone growth, non-invasive?

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

What is the FDA product code for Stimulator, bone growth, non-invasive?

The FDA product code for Stimulator, bone growth, non-invasive is LOF.

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Fuente oficial

Ver en la base de datos de la FDA →

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