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PMA de la FDA

STENT, SUPERFICIAL FEMORAL ARTERY

Número de PMA: P160025 · 2026-09-11

SolicitanteBiotronik AG
Fecha de decisión2026-09-11
Número PMAP160025
Código de productoNIP
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

STENT, SUPERFICIAL FEMORAL ARTERY is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik AG. It received FDA 510(k) clearance on 2026-09-11. The device is classified under product code NIP. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the STENT, SUPERFICIAL FEMORAL ARTERY?

STENT, SUPERFICIAL FEMORAL ARTERY is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Biotronik AG.

When did STENT, SUPERFICIAL FEMORAL ARTERY receive FDA 510(k) clearance?

The clearance date for STENT, SUPERFICIAL FEMORAL ARTERY can be found in the official FDA records.

Who is the listed applicant for STENT, SUPERFICIAL FEMORAL ARTERY?

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

What is the FDA product code for STENT, SUPERFICIAL FEMORAL ARTERY?

The FDA product code for STENT, SUPERFICIAL FEMORAL ARTERY is NIP.

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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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