510(k) K171140 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Matrixx System
| Applicant | Nexxt Spine, LLC, Noblesville IN, US |
| Decision | Substantially Equivalent, Aug 22, 2017 |
| Received | Apr 18, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171140
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.