510(k) K091813 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
INTREPID SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Nov 17, 2009 |
| Received | Jun 18, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091813
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.