510(k) K190363 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Omnia Medical TiBrid Cervical Cage, Omnia Medical TiBrid Lateral Cage, Omnia Medical TiBrid ALIF Cage, Omnia Medical TiBrid PLIF Cage, Omnia Medical TiBrid TLIF Cage
| Applicant | Omnia Medical, LLC, Morgantown, WV, US |
| Decision | Substantially Equivalent, Feb 21, 2020 |
| Received | Feb 15, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190363
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.