510(k) K172235 · LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
CoreHip® System
| Applicant | Aesculap Implants Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Mar 28, 2018 |
| Received | Jul 25, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172235
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.