510(k) K172086 · KWQ Appliance, Fixation, Spinal Intervertebral Body
Matira Anterior Cervical System
| Applicant | Kalitec Direct, LLC, Orlando FL, US |
| Decision | Substantially Equivalent, Sep 22, 2017 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172086
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.