510(k) K181792 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Duo Lumbar Interbody Fusion Device
| Applicant | Spineology, Inc., Saint Paul MN, US |
| Decision | Substantially Equivalent, Aug 14, 2018 |
| Received | Jul 5, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181792
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.