510(k) K024125 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
HALM ZIELKE INSTRUMENTATION SYSTEM
| Applicant | Micomed Ortho GmbH, San Diego CA, US |
| Decision | Substantially Equivalent, Sep 22, 2003 |
| Received | Dec 16, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024125
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.