FDA 510(k)

ArTT Augments and Buttresses and Bone Screws

N.º K: K251718 · 2025-08-29

Fecha de decisión2025-08-29

Código de productoLPH

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

ArTT Augments and Buttresses and Bone Screws is the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2025-08-29 under 510(k) number K251718. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ArTT Augments and Buttresses and Bone Screws?

ArTT Augments and Buttresses and Bone Screws is a medical device that received FDA 510(k) clearance on 2025-08-29. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K251718.

When did ArTT Augments and Buttresses and Bone Screws receive FDA 510(k) clearance?

ArTT Augments and Buttresses and Bone Screws received FDA 510(k) clearance on 2025-08-29, under 510(k) number K251718.

Who is the listed applicant for ArTT Augments and Buttresses and Bone Screws?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ArTT Augments and Buttresses and Bone Screws?

The FDA product code for ArTT Augments and Buttresses and Bone Screws is LPH.

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Otros registros que enlistan a Lima Corporate S.P.A. como solicitante

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Fuente oficial

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