510(k) K190890 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Exactech Alteon Modular Dual Mobility (MDM) System
| Applicant | Exactech, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Oct 22, 2019 |
| Received | Apr 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190890
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.