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PMA de la FDA

Scaffold, dissection repair

Número de PMA: P180034 · 2022-09-29

SolicitantePhilips Image Guided Therapy Corporation
Fecha de decisión2022-09-29
Número PMAP180034
Código de productoQCT
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorCV

Resumen del dispositivo

Scaffold, dissection repair is the device name listed in this FDA 510(k) record. The listed applicant is Philips Image Guided Therapy Corporation. It received FDA 510(k) clearance on 2022-09-29. The device is classified under product code QCT. It was reviewed by the CV advisory panel.

Preguntas frecuentes

What is the Scaffold, dissection repair?

Scaffold, dissection repair is a medical device that received FDA 510(k) clearance on 2022-09-29. The listed applicant is Philips Image Guided Therapy Corporation.

When did Scaffold, dissection repair receive FDA 510(k) clearance?

The clearance date for Scaffold, dissection repair can be found in the official FDA records.

Who is the listed applicant for Scaffold, dissection repair?

The FDA 510(k) record lists Philips Image Guided Therapy Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Scaffold, dissection repair?

The FDA product code for Scaffold, dissection repair is QCT.

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Fuente oficial

Ver en la base de datos de la FDA →

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