510(k) K061891 ยท MQP Spinal Vertebral Body Replacement Device
SYNEX II
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, Aug 18, 2006 |
| Received | Jul 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061891
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.