510(k) K121889 ยท MQP Spinal Vertebral Body Replacement Device
STAXX XD SYSTEM
| Applicant | Spine Wave, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Aug 29, 2012 |
| Received | Jun 28, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121889
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.