510(k) K001709 ยท JDQ Cerclage, Fixation
TROCHANTERIC REATTACHMENT DEVICE (STANDARD) AND (LONG), MODEL 501-066, 501-067
| Applicant | Pioneer Surgical Technology, Marquette MI, US |
| Decision | Substantially Equivalent, Aug 31, 2000 |
| Received | Jun 5, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001709
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.