PMA de la FDA

STENT, ILIAC

Número de PMA: P090006 · 2017-02-01

SolicitanteMedtronic Vascular

Fecha de decisión2017-02-01

Número PMAP090006

Código de productoNIO

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

STENT, ILIAC is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2017-02-01. The device is classified under product code NIO. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the STENT, ILIAC?

STENT, ILIAC is a medical device that received FDA 510(k) clearance on 2017-02-01. The listed applicant is Medtronic Vascular.

When did STENT, ILIAC receive FDA 510(k) clearance?

The clearance date for STENT, ILIAC can be found in the official FDA records.

Who is the listed applicant for STENT, ILIAC?

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

What is the FDA product code for STENT, ILIAC?

The FDA product code for STENT, ILIAC is NIO.

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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.