FDA 510(k)

Freedom Posterior Cervical Screws

Número K: K242674 · 2025-05-13

RequerenteSignature Orthopaedics Pty, Ltd.

Data da decisão2025-05-13

Código do produtoNKG

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Freedom Posterior Cervical Screws is the device name listed in this FDA 510(k) record. The listed applicant is Signature Orthopaedics Pty, Ltd.. It received FDA 510(k) clearance on 2025-05-13 under 510(k) number K242674. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Freedom Posterior Cervical Screws?

Freedom Posterior Cervical Screws is a medical device that received FDA 510(k) clearance on 2025-05-13. The listed applicant is Signature Orthopaedics Pty, Ltd.. The 510(k) number is K242674.

When did Freedom Posterior Cervical Screws receive FDA 510(k) clearance?

Freedom Posterior Cervical Screws received FDA 510(k) clearance on 2025-05-13, under 510(k) number K242674.

Who is the listed applicant for Freedom Posterior Cervical Screws?

The FDA 510(k) record lists Signature Orthopaedics Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Freedom Posterior Cervical Screws?

The FDA product code for Freedom Posterior Cervical Screws is NKG.

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Fonte oficial

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