510(k) K110864 ยท MQP Spinal Vertebral Body Replacement Device
BIOSPINE VBR SYSTEM
| Applicant | Aesculap Implant Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Jun 15, 2011 |
| Received | Mar 29, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110864
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.