510(k) K100889 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ENDOSKELETON TC
| Applicant | Titan Spine, LLC, Washington DC, US |
| Decision | Substantially Equivalent, Jul 29, 2010 |
| Received | Mar 31, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100889
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.