510(k) K173893 ยท PLR Spinal Vertebral Body Replacement Device - Cervical
Trabis
| Applicant | Coligne AG, Zurich, CH |
| Decision | Substantially Equivalent, Sep 6, 2018 |
| Received | Dec 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173893
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.