FDA 510(k)

MAVERICK External Fixation System

N.º K: K213874 · 2022-02-11

Fecha de decisión2022-02-11

Código de productoJDW

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

MAVERICK External Fixation System 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 2022-02-11 under 510(k) number K213874. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the MAVERICK External Fixation System?

MAVERICK External Fixation System is a medical device that received FDA 510(k) clearance on 2022-02-11. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K213874.

When did MAVERICK External Fixation System receive FDA 510(k) clearance?

MAVERICK External Fixation System received FDA 510(k) clearance on 2022-02-11, under 510(k) number K213874.

Who is the listed applicant for MAVERICK External Fixation System?

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 MAVERICK External Fixation System?

The FDA product code for MAVERICK External Fixation System is JDW.

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Otros registros que enlistan a Smith & Nephew, Inc. como solicitante

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Dispositivos relacionados (Código: JDW)

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Fuente oficial

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