FDA 510(k)

PMT Posterior Fixation System

N.º K: K172279 · 2017-09-20

SolicitanteProvidence Medical Technology, Inc.

Fecha de decisión2017-09-20

Código de productoNKG

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

PMT Posterior Fixation 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 2017-09-20 under 510(k) number K172279. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PMT Posterior Fixation System?

PMT Posterior Fixation System is a medical device that received FDA 510(k) clearance on 2017-09-20. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K172279.

When did PMT Posterior Fixation System receive FDA 510(k) clearance?

PMT Posterior Fixation System received FDA 510(k) clearance on 2017-09-20, under 510(k) number K172279.

Who is the listed applicant for PMT Posterior Fixation 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 PMT Posterior Fixation System?

The FDA product code for PMT Posterior Fixation System is NKG.

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Otros registros que enlistan a Providence Medical Technology, Inc. como solicitante

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Dispositivos relacionados (Código: NKG)

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Fuente oficial

Ver en la base de datos de la FDA →

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