510(k) K120038 ยท OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
A200 KNEE SYSTEM
| Applicant | Renovis Surgical Technologies, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 14, 2013 |
| Received | Jan 5, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120038
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.