510(k) K170206 ยท JDQ Cerclage, Fixation
Arthrex FiberTape Cerclage
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Nov 15, 2017 |
| Received | Jan 24, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170206
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.