510(k) K051027 ยท MQP Spinal Vertebral Body Replacement Device
STALIF TT
| Applicant | Surgicraft , Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, Jun 29, 2005 |
| Received | Apr 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051027
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.