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 a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2025-08-29 under approval 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. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K251718.
When was ArTT Augments and Buttresses and Bone Screws approved by the FDA?
ArTT Augments and Buttresses and Bone Screws received FDA 510(k) clearance on 2025-08-29, under approval number K251718.
What company makes ArTT Augments and Buttresses and Bone Screws?
ArTT Augments and Buttresses and Bone Screws is manufactured by Lima Corporate S.P.A..
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 Devices by Lima Corporate S.P.A.
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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.