510(k) K243809 · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Biolox® Delta Revision heads
| Applicant | Limacorporate, Villanova Di San Daniele Del Friuli, IT |
| Decision | Substantially Equivalent, Mar 4, 2025 |
| Received | Dec 11, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K243809
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.