FDA 510(k)

Reliance Cervical IBF System

Número K: K172489 · 2017-09-07

Data da decisão2017-09-07

Código do produtoODP

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Reliance Cervical IBF System is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Systems, LLC. It received FDA 510(k) clearance on 2017-09-07 under 510(k) number K172489. 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 Reliance Cervical IBF System?

Reliance Cervical IBF System is a medical device that received FDA 510(k) clearance on 2017-09-07. The listed applicant is Reliance Medical Systems, LLC. The 510(k) number is K172489.

When did Reliance Cervical IBF System receive FDA 510(k) clearance?

Reliance Cervical IBF System received FDA 510(k) clearance on 2017-09-07, under 510(k) number K172489.

Who is the listed applicant for Reliance Cervical IBF System?

The FDA 510(k) record lists Reliance Medical Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reliance Cervical IBF System?

The FDA product code for Reliance Cervical IBF System is ODP.

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Outros registros que listam Reliance Medical Systems, LLC como candidato(a)

K202266Reliance Cervical IBF System K210874Reliance Spinal Screw System K183049Reliance Lumbar IBF System K173283Reliance Lumbar IBF System K173102Reliance Cervical IBF System K162066Reliance Spinal Screw System

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Dispositivos Relacionados (Código: ODP)

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Fonte oficial

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