510(k) K991052 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
FS 1000 KNEE SYSTEM
| Applicant | Renaissance Instruments, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 10, 1999 |
| Received | Mar 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991052
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.