510(k) K171543 ยท OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
Renovis Surgical Hip Replacement System
| Applicant | Renovis Surgical Technologies, Redlands CA, US |
| Decision | Substantially Equivalent, Nov 16, 2017 |
| Received | May 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171543
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.