FDA 510(k)

Ceramic Femoral Head

Número K: K240452 · 2024-04-12

Data da decisão2024-04-12

Código do produtoLZO

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ceramic Femoral Head is the device name listed in this FDA 510(k) record. The listed applicant is Microport Orthopedics, Inc.. It received FDA 510(k) clearance on 2024-04-12 under 510(k) number K240452. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ceramic Femoral Head?

Ceramic Femoral Head is a medical device that received FDA 510(k) clearance on 2024-04-12. The listed applicant is Microport Orthopedics, Inc.. The 510(k) number is K240452.

When did Ceramic Femoral Head receive FDA 510(k) clearance?

Ceramic Femoral Head received FDA 510(k) clearance on 2024-04-12, under 510(k) number K240452.

Who is the listed applicant for Ceramic Femoral Head?

The FDA 510(k) record lists Microport Orthopedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ceramic Femoral Head?

The FDA product code for Ceramic Femoral Head is LZO.

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Fonte oficial

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