510(k) K171389 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
EVOLUTION Revision CCK System
| Applicant | Microport Orthopedics, Inc., Arlington TN, US |
| Decision | Substantially Equivalent, Aug 8, 2017 |
| Received | May 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171389
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.