510(k) K191408 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Nexxt Matrixx System
| Applicant | Nexxt Spine, LLC, Noblesville IN, US |
| Decision | Substantially Equivalent, Jul 10, 2019 |
| Received | May 28, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K191408
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.