510(k) K882241 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
KIRSCHNER (R) UNICONDYLAR-II KNEE SYSTEM
| Applicant | Kirschner Medical Corp., Timonium MD, US |
| Decision | Substantially Equivalent, Jun 29, 1988 |
| Received | May 27, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882241
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.