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PMA de la FDA

Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions

Número de PMA: P230023 · 2026-07-01

SolicitanteW. L. Gore & Associates, Inc.
Fecha de decisión2026-07-01
Número PMAP230023
Código de productoQZK
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions is the device name listed in this FDA 510(k) record. The listed applicant is W. L. Gore & Associates, Inc.. It received FDA 510(k) clearance on 2026-07-01. The device is classified under product code QZK. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions?

Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions is a medical device that received FDA 510(k) clearance on 2026-07-01. The listed applicant is W. L. Gore & Associates, Inc..

When did Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions receive FDA 510(k) clearance?

The clearance date for Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions can be found in the official FDA records.

Who is the listed applicant for Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions?

The FDA 510(k) record lists W. L. Gore & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions?

The FDA product code for Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions is QZK.

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Fuente oficial

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