510(k) K141635 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
ARTHREX IBALANCE TKA SYSTEM
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Sep 3, 2014 |
| Received | Jun 19, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141635
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.