Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PMA de la FDA

Iliac covered stent, arterial

Número de PMA: P160021 · 2026-06-16

SolicitanteW. L. Gore & Associates, Inc.
Fecha de decisión2026-06-16
Número PMAP160021
Código de productoPRL
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Iliac covered stent, arterial 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 2026-06-16. The device is classified under product code PRL. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Iliac covered stent, arterial?

Iliac covered stent, arterial is a medical device that received FDA 510(k) clearance on 2026-06-16. The listed applicant is W. L. Gore & Associates, Inc..

When did Iliac covered stent, arterial receive FDA 510(k) clearance?

The clearance date for Iliac covered stent, arterial can be found in the official FDA records.

Who is the listed applicant for Iliac covered stent, arterial?

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 Iliac covered stent, arterial?

The FDA product code for Iliac covered stent, arterial is PRL.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

↑