FDA 510(k)

LinkSymphoKnee System

Número K: K202924 · 2021-05-13

Data da decisão2021-05-13

Código do produtoJWH

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

LinkSymphoKnee System is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 2021-05-13 under 510(k) number K202924. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the LinkSymphoKnee System?

LinkSymphoKnee System is a medical device that received FDA 510(k) clearance on 2021-05-13. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K202924.

When did LinkSymphoKnee System receive FDA 510(k) clearance?

LinkSymphoKnee System received FDA 510(k) clearance on 2021-05-13, under 510(k) number K202924.

Who is the listed applicant for LinkSymphoKnee System?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LinkSymphoKnee System?

The FDA product code for LinkSymphoKnee System is JWH.

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Outros registros que listam Waldemar Link GmbH & Co. KG como candidato(a)

K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)K250375Allure Cadeira de Quadril e Plugs Intramedulares K243927MobileLink Acetabular Cup System - inhouse coatings K241636MobileLink Acetabular Cup System - Line Extension (Multiple)K231445LINK Embrace Shoulder System - Reverse Configuration K222066LINK MobileLink Acetabular Cup System

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Dispositivos Relacionados (Código: JWH)

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Fonte oficial

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