510(k) K072326 ยท MQP Spinal Vertebral Body Replacement Device
OSTAPEK VBR SYSTEM
| Applicant | Co-Ligne AG, Concord CA, US |
| Decision | Substantially Equivalent, Jun 24, 2008 |
| Received | Aug 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072326
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.