510(k) K983835 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
IMPLEX CONTINUUM PATELLA-REVISION HEDROCEL PATELLA
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Mar 15, 1999 |
| Received | Oct 30, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983835
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.