FDA 510(k)

C.A. Medical Interbody Fusion System

Número K: K254130 · 2026-07-08

Data da decisão2026-07-08

Código do produtoODP

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

C.A. Medical Interbody Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is C.A. Medical, LLC. It received FDA 510(k) clearance on 2026-07-08 under 510(k) number K254130. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the C.A. Medical Interbody Fusion System?

C.A. Medical Interbody Fusion System is a medical device that received FDA 510(k) clearance on 2026-07-08. The listed applicant is C.A. Medical, LLC. The 510(k) number is K254130.

When did C.A. Medical Interbody Fusion System receive FDA 510(k) clearance?

C.A. Medical Interbody Fusion System received FDA 510(k) clearance on 2026-07-08, under 510(k) number K254130.

Who is the listed applicant for C.A. Medical Interbody Fusion System?

The FDA 510(k) record lists C.A. Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C.A. Medical Interbody Fusion System?

The FDA product code for C.A. Medical Interbody Fusion System is ODP.

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Fonte oficial

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