510(k) K083186 ยท MQP Spinal Vertebral Body Replacement Device
AESCULAP HYDROLIFT VBR SYSTEM
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Mar 4, 2010 |
| Received | Oct 29, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083186
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.