510(k) K211837 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Altus Spine Interbody Standalone Fusion System
| Applicant | Altus Partners, LLC, West Chester PA, US |
| Decision | Substantially Equivalent, Apr 19, 2022 |
| Received | Jun 14, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211837
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.