510(k) K133802 ยท MQP Spinal Vertebral Body Replacement Device
AIS MODULIFT VBR SYSTEM
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Apr 17, 2014 |
| Received | Dec 13, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133802
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.