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FDA 510(k)

OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver

Número K: K230015 · 2023-06-16

RequerenteLaurane Medical Sas
Data da decisão2023-06-16
Código do produtoKNW
Comité consultivoGU
DecisãoSubstantially Equivalent

Resumo do dispositivo

OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver is the device name listed in this FDA 510(k) record. The listed applicant is Laurane Medical Sas. It received FDA 510(k) clearance on 2023-06-16 under 510(k) number K230015. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver?

OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver is a medical device that received FDA 510(k) clearance on 2023-06-16. The listed applicant is Laurane Medical Sas. The 510(k) number is K230015.

When did OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver receive FDA 510(k) clearance?

OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver received FDA 510(k) clearance on 2023-06-16, under 510(k) number K230015.

Who is the listed applicant for OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver?

The FDA 510(k) record lists Laurane Medical Sas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver?

The FDA product code for OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver is KNW.

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