510(k) K142996 ยท MQP Spinal Vertebral Body Replacement Device
StaXx(R) XD System
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Feb 19, 2015 |
| Received | Oct 16, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142996
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.