510(k) K251718 ยท LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
ArTT Augments and Buttresses and Bone Screws
| Applicant | Lima Corporate S.P.A., Villanova Di San Daniele, IT |
| Decision | Substantially Equivalent, Aug 29, 2025 |
| Received | Jun 4, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251718
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.