510(k) K112388 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
LANX CERVICAL SA
| Applicant | Lanx, Inc., Broomfield CO, US |
| Decision | Substantially Equivalent, Dec 16, 2011 |
| Received | Aug 18, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112388
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.