510(k) K161888 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
JULIET® LL Lateral Lumbar Cage
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Sep 12, 2016 |
| Received | Jul 11, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161888
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.