510(k) K122630 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
IN:C2 SPINAL FIXATION SYSTEM
| Applicant | Spine Smith Partners L.P., Austin TX, US |
| Decision | Substantially Equivalent, Dec 5, 2012 |
| Received | Aug 28, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122630
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.