510(k) K123388 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
K7C SPACER
| Applicant | K7, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Jan 4, 2013 |
| Received | Nov 2, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123388
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.