510(k) K190398 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Republic Spine Restore Intervertebral Body Fusion System
| Applicant | Republic Spine, LLC, Boca Raton FL, US |
| Decision | Substantially Equivalent, Sep 12, 2019 |
| Received | Feb 19, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190398
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.