510(k) K980781 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
IMPLEX CONTINUUM KNEE- HEDROCEL REVISION FEMORAL SPACERS
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, May 22, 1998 |
| Received | Mar 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980781
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.