510(k) K081888 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Feb 6, 2009 |
| Received | Jul 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081888
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.