FDA 510(k)

K5

Número K: K233805 · 2024-09-03

RequerenteOsstem Implant Co., Ltd. Chair Business

Data da decisão2024-09-03

Código do produtoEIA

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

K5 is the device name listed in this FDA 510(k) record. The listed applicant is Osstem Implant Co., Ltd. Chair Business. It received FDA 510(k) clearance on 2024-09-03 under 510(k) number K233805. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the K5?

K5 is a medical device that received FDA 510(k) clearance on 2024-09-03. The listed applicant is Osstem Implant Co., Ltd. Chair Business. The 510(k) number is K233805.

When did K5 receive FDA 510(k) clearance?

K5 received FDA 510(k) clearance on 2024-09-03, under 510(k) number K233805.

Who is the listed applicant for K5?

The FDA 510(k) record lists Osstem Implant Co., Ltd. Chair Business as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K5?

The FDA product code for K5 is EIA.

Dispositivos Relacionados (Código: EIA)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

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Fonte oficial

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