510(k) K070382 ยท MQP Spinal Vertebral Body Replacement Device
VISTA -S DEVICE
| Applicant | Zimmer Trabecular Metal Technology, Parsippany NJ, US |
| Decision | Substantially Equivalent, May 30, 2007 |
| Received | Feb 8, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070382
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.