510(k) K023983 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
MODIFICATION TO HIGHGATE CURVED ROD SYSTEM
| Applicant | Highgate Orthopaedics, Cleveland OH, US |
| Decision | Substantially Equivalent, Sep 22, 2003 |
| Received | Dec 2, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023983
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.