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PMA de la FDA

Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing

Número de PMA: P830055 · 2026-09-25

SolicitanteDepuy, Inc.
Fecha de decisión2026-09-25
Número PMAP830055
Código de productoNJL
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code NJL. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?

Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Depuy, Inc..

When did Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing receive FDA 510(k) clearance?

The clearance date for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing can be found in the official FDA records.

Who is the listed applicant for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?

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

What is the FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?

The FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is NJL.

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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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