510(k) K161226 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Revision Femoral Stem
| Applicant | Lima Corporate S.P.A., Villanova Di San Daniele Del Friuli, IT |
| Decision | Substantially Equivalent, Feb 10, 2017 |
| Received | May 2, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161226
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.