510(k) K180071 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STYLO Interbody Fusion Device
| Applicant | Legend Spine Technologies, Bethlehem PA, US |
| Decision | Substantially Equivalent, May 3, 2018 |
| Received | Jan 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180071
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.