510(k) K080349 ยท MQP Spinal Vertebral Body Replacement Device
KIMBA MINI
| Applicant | Signus Medizintechnik GmbH, Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 10, 2008 |
| Received | Feb 11, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080349
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.