510(k) K100516 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
ANYPLUS PEEK CAGES
| Applicant | GS Medical Co., Ltd., Douglassville PA, US |
| Decision | Substantially Equivalent, Dec 3, 2010 |
| Received | Feb 23, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100516
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.