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PMA de la FDA

Dispositivo de reparación de válvula tricúspide, administrado percutáneamente

Número de PMA: P230007 · 2026-06-25

SolicitanteABBOTT MEDICAL
Fecha de decisión2026-06-25
Número PMAP230007
Código de productoNPS
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Tricuspid valve repair device, percutaneously delivered is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2026-06-25. The device is classified under product code NPS. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Tricuspid valve repair device, percutaneously delivered?

Tricuspid valve repair device, percutaneously delivered is a medical device that received FDA 510(k) clearance on 2026-06-25. The listed applicant is ABBOTT MEDICAL.

When did Tricuspid valve repair device, percutaneously delivered receive FDA 510(k) clearance?

The clearance date for Tricuspid valve repair device, percutaneously delivered can be found in the official FDA records.

Who is the listed applicant for Tricuspid valve repair device, percutaneously delivered?

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

What is the FDA product code for Tricuspid valve repair device, percutaneously delivered?

The FDA product code for Tricuspid valve repair device, percutaneously delivered is NPS.

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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.

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