FDA 510(k)

ACCORD Cable System

N.º K: K233949 · 2024-03-13

Fecha de decisión2024-03-13

Código de productoJDQ

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

ACCORD Cable 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 2024-03-13 under 510(k) number K233949. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ACCORD Cable System?

ACCORD Cable System is a medical device that received FDA 510(k) clearance on 2024-03-13. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K233949.

When did ACCORD Cable System receive FDA 510(k) clearance?

ACCORD Cable System received FDA 510(k) clearance on 2024-03-13, under 510(k) number K233949.

Who is the listed applicant for ACCORD Cable 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 ACCORD Cable System?

The FDA product code for ACCORD Cable System is JDQ.

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Fuente oficial

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