510(k) K182085 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Balanced Knee Revision System Trabecular Tibial Cone Augments
| Applicant | Ortho Development Corporation, Draper UT, US |
| Decision | Substantially Equivalent, Oct 31, 2018 |
| Received | Aug 2, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182085
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.