510(k) K043020 ยท KWP Appliance, Fixation, Spinal Interlaminal
GLAXY 3.2 SPINAL SYSTEM
| Applicant | Medtronic Sofamor Danek, Memphis TN, US |
| Decision | Substantially Equivalent, Jan 7, 2005 |
| Received | Nov 3, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043020
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.