510(k) K190380 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
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| Applicant | Nvision Biomedical Technologies, Inc., San Antonio TX, US |
| Decision | Substantially Equivalent, Mar 21, 2019 |
| Received | Feb 19, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190380
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.