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PMA de la FDA

Stimulator, invasive bone growth

Número de PMA: P790005 · 2022-11-23

SolicitanteAhp Eos Buyer, Inc.
Fecha de decisión2022-11-23
Número PMAP790005
Código de productoLOE
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Stimulator, invasive bone growth is the device name listed in this FDA 510(k) record. The listed applicant is Ahp Eos Buyer, Inc.. It received FDA 510(k) clearance on 2022-11-23. The device is classified under product code LOE. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Stimulator, invasive bone growth?

Stimulator, invasive bone growth is a medical device that received FDA 510(k) clearance on 2022-11-23. The listed applicant is Ahp Eos Buyer, Inc..

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

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

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

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

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

The FDA product code for Stimulator, invasive bone growth is LOE.

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Fuente oficial

Ver en la base de datos de la FDA →

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