510(k) K133286 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
MIDLINE (TM)
| Applicant | Centinel Spine, Inc., West Chester PA, US |
| Decision | Substantially Equivalent, Jan 9, 2014 |
| Received | Oct 25, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K133286
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.