FDA 510(k)

CAVUX™ Cervical Cage

Número K: K161642 · 2016-10-07

RequerenteProvidence Medical Technology, Inc.

Data da decisão2016-10-07

Código do produtoODP

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

CAVUX™ Cervical Cage 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 2016-10-07 under 510(k) number K161642. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the CAVUX™ Cervical Cage?

CAVUX™ Cervical Cage is a medical device that received FDA 510(k) clearance on 2016-10-07. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K161642.

When did CAVUX™ Cervical Cage receive FDA 510(k) clearance?

CAVUX™ Cervical Cage received FDA 510(k) clearance on 2016-10-07, under 510(k) number K161642.

Who is the listed applicant for CAVUX™ Cervical Cage?

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™ Cervical Cage?

The FDA product code for CAVUX™ Cervical Cage is ODP.

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Outros registros que listam Providence Medical Technology, Inc. como candidato(a)

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Dispositivos Relacionados (Código: ODP)

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Fonte oficial

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