510(k) K200541 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Hive Stand-alone Anterior Lumbar Interbody System
| Applicant | Hd Lifesciences, LLC, Woburn MA, US |
| Decision | Substantially Equivalent, Apr 28, 2020 |
| Received | Mar 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200541
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.