510(k) K073109 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
STALIF TT INTERVERTEBRAL BODY FUSION SYSTEM
| Applicant | Surgicraft , Ltd., Douglassville PA, US |
| Decision | Substantially Equivalent, Jun 4, 2008 |
| Received | Nov 2, 2007 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K073109
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.