510(k) K053579 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
COLUMBUS ULTRA CONGRUENT (UC) TIBIAL INSERT/GLIDING SURFACE
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, May 17, 2006 |
| Received | Dec 22, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053579
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.