510(k) K133328 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
AERO-AL LUMBAR CAGE SYSTEM
| Applicant | Stryker Corporation, Allendale NJ, US |
| Decision | Substantially Equivalent, May 30, 2014 |
| Received | Oct 29, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133328
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.