510(k) K181702 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Tranquil-L Interbody System
| Applicant | Nexus Spine, LLC, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 21, 2018 |
| Received | Jun 27, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181702
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.