510(k) K042859 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
KOBRA GPS FIXATION SYSTEM
| Applicant | Medtronic Vertelink, Inc., Mission Viejo CA, US |
| Decision | Substantially Equivalent, Nov 24, 2004 |
| Received | Oct 15, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042859
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.