510(k) K070883 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
DURACON X3 CS TIBIAL INSERT
| Applicant | Howmedica Osteonics Corp., Mahwah NJ, US |
| Decision | Substantially Equivalent, May 11, 2007 |
| Received | Mar 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070883
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.