510(k) K110153 ยท MQP Spinal Vertebral Body Replacement Device
SFC VERTEBRAL BODY REPLACEMENT
| Applicant | Konigsee Implantate GmbH, Washington DC, US |
| Decision | Substantially Equivalent, Oct 12, 2011 |
| Received | Jan 19, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110153
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.