510(k) K051039 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
BASIS SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek USA, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, May 12, 2005 |
| Received | Apr 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051039
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.