510(k) K210590 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Axis Spine Technologies ALIF
| Applicant | Axis Spine Technologies, Ltd., St. Albans, GB |
| Decision | Substantially Equivalent, Sep 29, 2021 |
| Received | Mar 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210590
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.