510(k) K090315 ยท MQP Spinal Vertebral Body Replacement Device
STAXX XD SYSTEM
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Sep 3, 2009 |
| Received | Feb 9, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090315
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.