510(k) K103382 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
INTERCONTINENTAL PLATE-SPACER
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, May 20, 2011 |
| Received | Nov 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103382
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.