510(k) K031782 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
GAPP GRAFT CONTIANMENT DEVICE ORTHOPEDICS
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Feb 1, 2005 |
| Received | Jun 10, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031782
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.