510(k) K180519 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
HARRIER-SA Lumbar Interbody System
| Applicant | Choicespine, LP, Knoxville TN, US |
| Decision | Substantially Equivalent, May 16, 2018 |
| Received | Feb 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180519
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.