FDA 510(k)

FasTouch Absorbable Fixation System

Número K: K181668 · 2019-03-13

Data da decisão2019-03-13

Código do produtoGDW

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

FasTouch Absorbable Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Via Surgical , Ltd.. It received FDA 510(k) clearance on 2019-03-13 under 510(k) number K181668. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the FasTouch Absorbable Fixation System?

FasTouch Absorbable Fixation System is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Via Surgical , Ltd.. The 510(k) number is K181668.

When did FasTouch Absorbable Fixation System receive FDA 510(k) clearance?

FasTouch Absorbable Fixation System received FDA 510(k) clearance on 2019-03-13, under 510(k) number K181668.

Who is the listed applicant for FasTouch Absorbable Fixation System?

The FDA 510(k) record lists Via Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FasTouch Absorbable Fixation System?

The FDA product code for FasTouch Absorbable Fixation System is GDW.

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Outros registros que listam Via Surgical , Ltd. como candidato(a)

K203117TissueTak device K162252FasTouch Fixation System

Dispositivos Relacionados (Código: GDW)

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