510(k) K081351 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
MODIFICATION TO JOURNEY UNICONDYLAR FEMORAL IMPLANT
| Applicant | Smith & Nephew, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jul 24, 2008 |
| Received | May 14, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081351
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.