FDA 510(k)

Double Medical Cage System

Número K: K172828 · 2018-02-01

RequerenteDouble Medical Technology, Inc.

Data da decisão2018-02-01

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Double Medical Cage System is the device name listed in this FDA 510(k) record. The listed applicant is Double Medical Technology, Inc.. It received FDA 510(k) clearance on 2018-02-01 under 510(k) number K172828. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Double Medical Cage System?

Double Medical Cage System is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Double Medical Technology, Inc.. The 510(k) number is K172828.

When did Double Medical Cage System receive FDA 510(k) clearance?

Double Medical Cage System received FDA 510(k) clearance on 2018-02-01, under 510(k) number K172828.

Who is the listed applicant for Double Medical Cage System?

The FDA 510(k) record lists Double Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Double Medical Cage System?

The FDA product code for Double Medical Cage System is MAX.

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Fonte oficial

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