FDA 510(k)

Libertas Acetabular Hooded Liner

Número K: K183365 · 2019-02-22

Data da decisão2019-02-22

Código do produtoLZO

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Libertas Acetabular Hooded Liner is the device name listed in this FDA 510(k) record. The listed applicant is Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2019-02-22 under 510(k) number K183365. 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 Libertas Acetabular Hooded Liner?

Libertas Acetabular Hooded Liner is a medical device that received FDA 510(k) clearance on 2019-02-22. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K183365.

When did Libertas Acetabular Hooded Liner receive FDA 510(k) clearance?

Libertas Acetabular Hooded Liner received FDA 510(k) clearance on 2019-02-22, under 510(k) number K183365.

Who is the listed applicant for Libertas Acetabular Hooded Liner?

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

What is the FDA product code for Libertas Acetabular Hooded Liner?

The FDA product code for Libertas Acetabular Hooded Liner is LZO.

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Outros registros que listam Maxx Orthopedics, Inc. como candidato(a)

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Fonte oficial

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