510(k) K052170 ยท MQP Spinal Vertebral Body Replacement Device
SEASPINE VBR SYSTEM
| Applicant | Seaspine, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Dec 21, 2005 |
| Received | Aug 9, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052170
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.