510(k) K953443 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
CONSENSUS PCL SUBSITUTING TIBIAL INSERT
| Applicant | U.S. Medical Products, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Apr 26, 1996 |
| Received | Jul 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953443
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.