510(k) K013982 ยท KRR Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer
KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT
| Applicant | Kinamed, Inc., Camarillo CA, US |
| Decision | Substantially Equivalent, May 21, 2002 |
| Received | Dec 3, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013982
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.