510(k) K102067 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ENDOSKELETON TO
| Applicant | Titan Spine, LLC, Apple Valley MN, US |
| Decision | Substantially Equivalent, Nov 5, 2010 |
| Received | Jul 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102067
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.