510(k) K930831 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
MG II POROUS KNEE SYSTEM FEMORAL COMPONENTS
| Applicant | Zimmer, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Nov 16, 1993 |
| Received | Feb 17, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930831
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.