510(k) K032102 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
VERTELINK KOBRA SPINAL FIXATION SYSTEM
| Applicant | Vertelink Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, Dec 12, 2003 |
| Received | Jul 8, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032102
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.