510(k) K200338 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ProLift Lateral Fixated
| Applicant | Life Spine, Inc., Huntley IL, US |
| Decision | Substantially Equivalent, Apr 17, 2020 |
| Received | Feb 11, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200338
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.