510(k) K081968 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
MODIFICATION TO LUCENT
| Applicant | Spinal Elements, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 5, 2008 |
| Received | Jul 10, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081968
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.