510(k) K073320 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
CIMPLICITY SPINAL SYSTEM
| Applicant | Spine Smith Partners L.P., Austin TX, US |
| Decision | Substantially Equivalent, Feb 7, 2008 |
| Received | Nov 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073320
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.