K251718
- 510(k) number
- K251718
- Device name
- ArTT Augments and Buttresses and Bone Screws
- Applicant
- Lima Corporate S.P.A. IT
- Product code
- LPH — Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Po
- Decision date
- 2025-08-29
- Date received
- 2025-06-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K251718.pdf
Official FDA record: K251718
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.