510(k) K072029 ยท MQP Spinal Vertebral Body Replacement Device
PHENIX VERTEBRAL BODY REPLACEMENT
| Applicant | New Business Development, LLC, Marietta GA, US |
| Decision | Substantially Equivalent, Oct 15, 2007 |
| Received | Jul 24, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072029
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.