510(k) K020152 ยท MQP Spinal Vertebral Body Replacement Device
SYNTHES VERTEBRAL SPACER TI
| Applicant | Synthes (Usa), Paoli PA, US |
| Decision | Substantially Equivalent, Apr 16, 2002 |
| Received | Jan 17, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020152
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.