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PMA de la FDA

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

Número de PMA: P030022 · 2022-08-08

SolicitanteSmith & Nephew, Inc.
Fecha de decisión2022-08-08
Número PMAP030022
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 Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-08-08. 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 2022-08-08. The listed applicant is Smith & Nephew, 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 Smith & Nephew, 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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