FDA 510(k)

CPM Medical Consultants Tibial Revision Knee System

N.º K: K210695 · 2021-08-16

Fecha de decisión2021-08-16

Código de productoJWH

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

CPM Medical Consultants Tibial Revision Knee System is the device name listed in this FDA 510(k) record. The listed applicant is Cpm Medical Consultants, LLC. It received FDA 510(k) clearance on 2021-08-16 under 510(k) number K210695. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CPM Medical Consultants Tibial Revision Knee System?

CPM Medical Consultants Tibial Revision Knee System is a medical device that received FDA 510(k) clearance on 2021-08-16. The listed applicant is Cpm Medical Consultants, LLC. The 510(k) number is K210695.

When did CPM Medical Consultants Tibial Revision Knee System receive FDA 510(k) clearance?

CPM Medical Consultants Tibial Revision Knee System received FDA 510(k) clearance on 2021-08-16, under 510(k) number K210695.

Who is the listed applicant for CPM Medical Consultants Tibial Revision Knee System?

The FDA 510(k) record lists Cpm Medical Consultants, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPM Medical Consultants Tibial Revision Knee System?

The FDA product code for CPM Medical Consultants Tibial Revision Knee System is JWH.

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Dispositivos relacionados (Código: JWH)

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Fuente oficial

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