510(k) K820995 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
MAGNE-FIELD 400D OSTEO-BIO-NETIC SYS
| Applicant | Ludek Optics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 25, 1982 |
| Received | Apr 9, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820995
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.