510(k) K131472 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
APEX KNEE MODULAR TIBIA SYSTEM
| Applicant | Omni Life Science, Inc., East Taunton MA, US |
| Decision | Substantially Equivalent, Oct 8, 2013 |
| Received | May 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131472
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.