510(k) K152302 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Xenco Medical Cervical Interbody System (Argus)
| Applicant | Xenco Medical, LLC, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 10, 2015 |
| Received | Aug 14, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K152302
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.