510(k) K142328 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
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| Applicant | Nvision Biomedical Technologies, LLC, San Antonio TN, US |
| Decision | Substantially Equivalent, Dec 23, 2014 |
| Received | Aug 20, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142328
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.