510(k) K071726 ยท MQP Spinal Vertebral Body Replacement Device
ZUMA
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Oct 23, 2007 |
| Received | Jun 25, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071726
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.