FDA 510(k)

Piccolo Composite Proximal Tibia Plate System

Número K: K201917 · 2020-10-08

Data da decisão2020-10-08

Código do produtoHRS

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Piccolo Composite Proximal Tibia Plate System is the device name listed in this FDA 510(k) record. The listed applicant is CarboFix Orthopedics , Ltd.. It received FDA 510(k) clearance on 2020-10-08 under 510(k) number K201917. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Piccolo Composite Proximal Tibia Plate System?

Piccolo Composite Proximal Tibia Plate System is a medical device that received FDA 510(k) clearance on 2020-10-08. The listed applicant is CarboFix Orthopedics , Ltd.. The 510(k) number is K201917.

When did Piccolo Composite Proximal Tibia Plate System receive FDA 510(k) clearance?

Piccolo Composite Proximal Tibia Plate System received FDA 510(k) clearance on 2020-10-08, under 510(k) number K201917.

Who is the listed applicant for Piccolo Composite Proximal Tibia Plate System?

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

What is the FDA product code for Piccolo Composite Proximal Tibia Plate System?

The FDA product code for Piccolo Composite Proximal Tibia Plate System is HRS.

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Fonte oficial

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