FDA 510(k)

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System

Número K: K151848 · 2016-01-15

Data da decisão2016-01-15

Código do produtoJDQ

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2016-01-15 under 510(k) number K151848. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is a medical device that received FDA 510(k) clearance on 2016-01-15. The listed applicant is Zimmer, Inc.. The 510(k) number is K151848.

When did Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System receive FDA 510(k) clearance?

Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System received FDA 510(k) clearance on 2016-01-15, under 510(k) number K151848.

Who is the listed applicant for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

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

What is the FDA product code for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System?

The FDA product code for Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System is JDQ.

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Fonte oficial

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