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PMA de la FDA

Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented

Número de PMA: P070026 · 2026-09-04

SolicitanteDePuy Orthopaedics, Inc.
Fecha de decisión2026-09-04
Número PMAP070026
Código de productoMRA
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2026-09-04. The device is classified under product code MRA. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?

Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is a medical device that received FDA 510(k) clearance on 2026-09-04. The listed applicant is DePuy Orthopaedics, Inc..

When did Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented receive FDA 510(k) clearance?

The clearance date for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented can be found in the official FDA records.

Who is the listed applicant for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?

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

What is the FDA product code for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented?

The FDA product code for Prosthesis, hip, semi-constrained, metal/ceramic/ceramic/metal, cemented or uncemented is MRA.

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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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