510(k) K102315 ยท MQP Spinal Vertebral Body Replacement Device
STAXX XDL SYSTEM
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Aug 19, 2011 |
| Received | Aug 16, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102315
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.