510(k) K152011 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Lucent Intervertebral Body Fusion Device
| Applicant | Spinal Elements, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Jun 9, 2016 |
| Received | Jul 21, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152011
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.