FDA 510(k)

Libertas Hip Replacement System

N.º K: K180973 · 2018-09-28

Fecha de decisión2018-09-28

Código de productoJDI

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Libertas Hip Replacement System is the device name listed in this FDA 510(k) record. The listed applicant is Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2018-09-28 under 510(k) number K180973. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Libertas Hip Replacement System?

Libertas Hip Replacement System is a medical device that received FDA 510(k) clearance on 2018-09-28. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K180973.

When did Libertas Hip Replacement System receive FDA 510(k) clearance?

Libertas Hip Replacement System received FDA 510(k) clearance on 2018-09-28, under 510(k) number K180973.

Who is the listed applicant for Libertas Hip Replacement System?

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

What is the FDA product code for Libertas Hip Replacement System?

The FDA product code for Libertas Hip Replacement System is JDI.

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Otros registros que enlistan a Maxx Orthopedics, Inc. como solicitante

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Dispositivos relacionados (Código: JDI)

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Fuente oficial

Ver en la base de datos de la FDA →

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