510(k) K191791 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
TranS1 Interbody Fusion System
| Applicant | Trans1, Wilmington NC, US |
| Decision | Substantially Equivalent, Sep 25, 2019 |
| Received | Jul 3, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191791
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.