510(k) K083167 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
PHENIX CERVICAL INTERBODY DEVICE
| Applicant | Spinal Devices, LLC, Apple Valley MN, US |
| Decision | Substantially Equivalent, Jan 13, 2009 |
| Received | Oct 27, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083167
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.