510(k) K220610 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SOLO-L
| Applicant | Aurora Spine, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 27, 2022 |
| Received | Mar 3, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220610
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.