510(k) K230808 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System
| Applicant | Kyocera Medical Technologies, Inc., Redlands CA, US |
| Decision | Substantially Equivalent, Apr 21, 2023 |
| Received | Mar 23, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230808
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.