510(k) K982302 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
IMPLEX CONTINUUM KNEE - HEDROCEL TIBIAL SPACERS
| Applicant | Implex Corp., Allendale NJ, US |
| Decision | Substantially Equivalent for Some Indications, Jul 31, 1998 |
| Received | Jul 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982302
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.