510(k) K062083 ยท MQP Spinal Vertebral Body Replacement Device
SYNFIX -LR
| Applicant | Synthes Spine Co.Lp, West Chester PA, US |
| Decision | Substantially Equivalent, Apr 3, 2007 |
| Received | Jul 21, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062083
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.