510(k) K133342 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ARTHREX IBALANCE TKA SYSTEM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Dec 17, 2013 |
| Received | Oct 30, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133342
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.