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FDA 510(k)

ArTT Augments and Buttresses and Bone Screws

K-Number: K251718 · 2025-08-29

ApplicantLima Corporate S.P.A.
Decision Date2025-08-29
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Lima Corporate S.P.A. as applicant

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Related Devices (Code: LPH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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