510(k) K182322 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Duo Lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Oct 24, 2018 |
| Received | Aug 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182322
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.