510(k) K141942 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
MIDLINE II TI
| Applicant | Centinel Spine, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Nov 7, 2014 |
| Received | Jul 17, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141942
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.