510(k) K082252 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
INDEPENDENCE SPACER
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Nov 5, 2008 |
| Received | Aug 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082252
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.