510(k) K990345 ยท JDK Prosthesis, Hip, Cement Restrictor
RABEA DEVICE, MODEL PXXXXXX
| Applicant | Signus Medizintechnik GmbH, Shorewood MN, US |
| Decision | Unknown, Jul 30, 1999 |
| Received | Feb 4, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990345
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.