PMA de la FDA

Aórtico estent

Número de PMA: P240003 · 2026-08-27

SolicitanteRenata Medical, Inc.

Fecha de decisión2026-08-27

Número PMAP240003

Código de productoPNF

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorCV

Resumen del dispositivo

Aortic stent is the device name listed in this FDA 510(k) record. The listed applicant is Renata Medical, Inc.. It received FDA 510(k) clearance on 2026-08-27. The device is classified under product code PNF. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Aortic stent?

Aortic stent is a medical device that received FDA 510(k) clearance on 2026-08-27. The listed applicant is Renata Medical, Inc..

When did Aortic stent receive FDA 510(k) clearance?

The clearance date for Aortic stent can be found in the official FDA records.

Who is the listed applicant for Aortic stent?

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

What is the FDA product code for Aortic stent?

The FDA product code for Aortic stent is PNF.

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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.