FDA 510(k)

Trinity EVO Acetabular Shell

Número K: K242744 · 2025-06-05

Data da decisão2025-06-05

Código do produtoLPH

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Trinity EVO Acetabular Shell is the device name listed in this FDA 510(k) record. The listed applicant is Corin U.S.A. Limited. It received FDA 510(k) clearance on 2025-06-05 under 510(k) number K242744. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Trinity EVO Acetabular Shell?

Trinity EVO Acetabular Shell is a medical device that received FDA 510(k) clearance on 2025-06-05. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K242744.

When did Trinity EVO Acetabular Shell receive FDA 510(k) clearance?

Trinity EVO Acetabular Shell received FDA 510(k) clearance on 2025-06-05, under 510(k) number K242744.

Who is the listed applicant for Trinity EVO Acetabular Shell?

The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Trinity EVO Acetabular Shell?

The FDA product code for Trinity EVO Acetabular Shell is LPH.

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Fonte oficial

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