510(k) K120869 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ANCHOR-L LUMBAR CAGE
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Oct 25, 2012 |
| Received | Mar 22, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120869
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.