FDA 510(k)

Longeviti ClearFit Cranial Implant

Número K: K202901 · 2020-10-30

RequerenteLongeviti Neuro Solutions, LLC

Data da decisão2020-10-30

Código do produtoGXN

Comité consultivoNE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Longeviti ClearFit Cranial Implant is the device name listed in this FDA 510(k) record. The listed applicant is Longeviti Neuro Solutions, LLC. It received FDA 510(k) clearance on 2020-10-30 under 510(k) number K202901. The device is classified under product code GXN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Longeviti ClearFit Cranial Implant?

Longeviti ClearFit Cranial Implant is a medical device that received FDA 510(k) clearance on 2020-10-30. The listed applicant is Longeviti Neuro Solutions, LLC. The 510(k) number is K202901.

When did Longeviti ClearFit Cranial Implant receive FDA 510(k) clearance?

Longeviti ClearFit Cranial Implant received FDA 510(k) clearance on 2020-10-30, under 510(k) number K202901.

Who is the listed applicant for Longeviti ClearFit Cranial Implant?

The FDA 510(k) record lists Longeviti Neuro Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Longeviti ClearFit Cranial Implant?

The FDA product code for Longeviti ClearFit Cranial Implant is GXN.

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Outros registros que listam Longeviti Neuro Solutions, LLC como candidato(a)

K231920Longeviti ClearFit OTS Cranial Implant K212058Longeviti ClearFit™ OTS Cranial Implants K211514Longeviti PorousFit implant K210616Longeviti PMMA Static Cranial Implant K203349Longeviti ClearFit Cranial Implant K191210Longeviti ClearFit Cranial Implant

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Dispositivos Relacionados (Código: GXN)

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Fonte oficial

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