510(k) K153621 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Juliet® Ti
| Applicant | Spineart, Geneva, CH |
| Decision | Substantially Equivalent, Jul 15, 2016 |
| Received | Dec 18, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K153621
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 22, 2019 | SPINEART SA Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures Terminated |
MAX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.