510(k) K101720 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
JULIET OL
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Jul 16, 2010 |
| Received | Jun 18, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101720
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.