510(k) K150581 ยท JDQ Cerclage, Fixation
Tritium Sternal Cable Plate System
| Applicant | Pioneer Surgical Technology, Inc. (Dba Rti Surgical, Inc.), Marquette MI, US |
| Decision | Substantially Equivalent, Jun 4, 2015 |
| Received | Mar 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150581
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.