FDA 510(k)

DePuy Synthes 2.7mm VA LCP Clavicle Plate System

N.º K: K201321 · 2020-07-24

Fecha de decisión2020-07-24

Código de productoHRS

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

DePuy Synthes 2.7mm VA LCP Clavicle Plate System is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Synthes. It received FDA 510(k) clearance on 2020-07-24 under 510(k) number K201321. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

DePuy Synthes 2.7mm VA LCP Clavicle Plate System is a medical device that received FDA 510(k) clearance on 2020-07-24. The listed applicant is DePuy Synthes. The 510(k) number is K201321.

When did DePuy Synthes 2.7mm VA LCP Clavicle Plate System receive FDA 510(k) clearance?

DePuy Synthes 2.7mm VA LCP Clavicle Plate System received FDA 510(k) clearance on 2020-07-24, under 510(k) number K201321.

Who is the listed applicant for DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

The FDA 510(k) record lists DePuy Synthes as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DePuy Synthes 2.7mm VA LCP Clavicle Plate System?

The FDA product code for DePuy Synthes 2.7mm VA LCP Clavicle Plate System is HRS.

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Fuente oficial

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