510(k) K041617 ยท MQP Spinal Vertebral Body Replacement Device
STALIF TT
| Applicant | Surgicraft , Ltd., Chicago IL, US |
| Decision | Substantially Equivalent, Sep 8, 2004 |
| Received | Jun 15, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041617
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.