FDA 510(k)

CAVUX CervicalCage-L SA System

Número K: K163474 · 2017-03-10

RequerenteProvidence Medical Technology, Inc.

Data da decisão2017-03-10

Código do produtoOVE

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

CAVUX CervicalCage-L SA System is the device name listed in this FDA 510(k) record. The listed applicant is Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2017-03-10 under 510(k) number K163474. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the CAVUX CervicalCage-L SA System?

CAVUX CervicalCage-L SA System is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K163474.

When did CAVUX CervicalCage-L SA System receive FDA 510(k) clearance?

CAVUX CervicalCage-L SA System received FDA 510(k) clearance on 2017-03-10, under 510(k) number K163474.

Who is the listed applicant for CAVUX CervicalCage-L SA System?

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

What is the FDA product code for CAVUX CervicalCage-L SA System?

The FDA product code for CAVUX CervicalCage-L SA System is OVE.

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Fonte oficial

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