510(k) K150643 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti
| Applicant | Centinel Spine, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, Jun 8, 2015 |
| Received | Mar 12, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150643
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.