FDA 510(k)

MAVERICK Mini External Fixation System

N.º K: K223112 · 2022-12-08

Fecha de decisión2022-12-08

Código de productoJDW

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

MAVERICK Mini 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 2022-12-08 under 510(k) number K223112. 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 Mini External Fixation System?

MAVERICK Mini External Fixation System is a medical device that received FDA 510(k) clearance on 2022-12-08. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K223112.

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

MAVERICK Mini External Fixation System received FDA 510(k) clearance on 2022-12-08, under 510(k) number K223112.

Who is the listed applicant for MAVERICK Mini 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 Mini External Fixation System?

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

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

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Fuente oficial

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