510(k) K181397 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
DualX
| Applicant | Innovasive, Inc., Mission Viejo CA, US |
| Decision | Substantially Equivalent, Sep 27, 2018 |
| Received | May 29, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181397
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.