FDA 510(k)

SpineView X-Pac Expandable Lumbar Cage System

Número K: K152539 · 2016-02-24

Data da decisão2016-02-24

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

SpineView X-Pac Expandable Lumbar Cage System is the device name listed in this FDA 510(k) record. The listed applicant is Spine View, Inc.. It received FDA 510(k) clearance on 2016-02-24 under 510(k) number K152539. 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 SpineView X-Pac Expandable Lumbar Cage System?

SpineView X-Pac Expandable Lumbar Cage System is a medical device that received FDA 510(k) clearance on 2016-02-24. The listed applicant is Spine View, Inc.. The 510(k) number is K152539.

When did SpineView X-Pac Expandable Lumbar Cage System receive FDA 510(k) clearance?

SpineView X-Pac Expandable Lumbar Cage System received FDA 510(k) clearance on 2016-02-24, under 510(k) number K152539.

Who is the listed applicant for SpineView X-Pac Expandable Lumbar Cage System?

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

What is the FDA product code for SpineView X-Pac Expandable Lumbar Cage System?

The FDA product code for SpineView X-Pac Expandable Lumbar Cage System is MAX.

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Outros registros que listam Spine View, Inc. como candidato(a)

K160856SpineView X-Pac Expandable Lumbar Cage System

Dispositivos Relacionados (Código: MAX)

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Fonte oficial

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