510(k) K172083 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Idys ALIF System
| Applicant | Clariance, Sas, Beaurains, FR |
| Decision | Substantially Equivalent, Nov 8, 2017 |
| Received | Jul 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172083
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.