510(k) K120031 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
CHESAPEAKE SPINAL SYSTEM
| Applicant | K2m, Inc., Leesburg VA, US |
| Decision | Substantially Equivalent, Mar 16, 2012 |
| Received | Jan 4, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120031
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.