510(k) K893762 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
PLUS TOTAL KNEE SYSTEM, (PPD) TIBIAL COMPONENT
| Applicant | Orthomet, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent for Some Indications, Sep 15, 1989 |
| Received | May 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893762
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.