510(k) K042713 ยท MQP Spinal Vertebral Body Replacement Device
FIDJI-VERTEBRAL BODY REPLACEMENT TYPE 5
| Applicant | Spine Next America Corporation, Jacksonville FL, US |
| Decision | Substantially Equivalent, Dec 29, 2004 |
| Received | Sep 30, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042713
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.