FDA 510(k)

Medussa-PL Cage

Número K: K223654 · 2022-12-28

Data da decisão2022-12-28

Código do produtoMAX

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Medussa-PL Cage is the device name listed in this FDA 510(k) record. The listed applicant is Medyssey USA, Inc.. It received FDA 510(k) clearance on 2022-12-28 under 510(k) number K223654. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Medussa-PL Cage?

Medussa-PL Cage is a medical device that received FDA 510(k) clearance on 2022-12-28. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K223654.

When did Medussa-PL Cage receive FDA 510(k) clearance?

Medussa-PL Cage received FDA 510(k) clearance on 2022-12-28, under 510(k) number K223654.

Who is the listed applicant for Medussa-PL Cage?

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

What is the FDA product code for Medussa-PL Cage?

The FDA product code for Medussa-PL Cage is MAX.

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Fonte oficial

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