510(k) K831512 ยท JDK Prosthesis, Hip, Cement Restrictor
DOSIMETRY RELEASE OF RADIATION STERILIZ
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 29, 1983 |
| Received | May 12, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831512
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.