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FDA 510(k)

Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix

Número K: K190378 · 2019-05-24

RequerenteBioncise NV
Data da decisão2019-05-24
Código do produtoKNW
Comité consultivoGU
DecisãoSubstantially Equivalent

Resumo do dispositivo

Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix is the device name listed in this FDA 510(k) record. The listed applicant is Bioncise NV. It received FDA 510(k) clearance on 2019-05-24 under 510(k) number K190378. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?

Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix is a medical device that received FDA 510(k) clearance on 2019-05-24. The listed applicant is Bioncise NV. The 510(k) number is K190378.

When did Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix receive FDA 510(k) clearance?

Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix received FDA 510(k) clearance on 2019-05-24, under 510(k) number K190378.

Who is the listed applicant for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?

The FDA 510(k) record lists Bioncise NV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix?

The FDA product code for Spirotome Endo 08 Gauge, Spirotome Endo 10 Gauge, Spirotome Endo 14 Gauge, Spirotome Endo 14 Gauge with 10 mm Helix is KNW.

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