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PMA de la FDA

Implant, resorbable, for articular osteochondral repair

Número de PMA: P210034 · 2026-06-04

SolicitanteSmith and Nephew, Inc.
Fecha de decisión2026-06-04
Número PMAP210034
Código de productoQRU
Clase del dispositivoClase 3
Especialidad médicaU
Comité asesorOR

Resumen del dispositivo

Implant, resorbable, for articular osteochondral repair is the device name listed in this FDA 510(k) record. The listed applicant is Smith and Nephew, Inc.. It received FDA 510(k) clearance on 2026-06-04. The device is classified under product code QRU. It was reviewed by the OR advisory panel.

Preguntas frecuentes

What is the Implant, resorbable, for articular osteochondral repair?

Implant, resorbable, for articular osteochondral repair is a medical device that received FDA 510(k) clearance on 2026-06-04. The listed applicant is Smith and Nephew, Inc..

When did Implant, resorbable, for articular osteochondral repair receive FDA 510(k) clearance?

The clearance date for Implant, resorbable, for articular osteochondral repair can be found in the official FDA records.

Who is the listed applicant for Implant, resorbable, for articular osteochondral repair?

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

What is the FDA product code for Implant, resorbable, for articular osteochondral repair?

The FDA product code for Implant, resorbable, for articular osteochondral repair is QRU.

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Fuente oficial

Ver en la base de datos de la FDA →

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