510(k) K140055 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ENDOSKELETON(R) TL INTERBODY FUSION DEVICE
| Applicant | Titan Spine, LLC, Bartlett TN, US |
| Decision | Substantially Equivalent, Jul 2, 2014 |
| Received | Jan 10, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140055
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.