510(k) K042317 ยท KWQ Appliance, Fixation, Spinal Intervertebral Body
CERVICAL PLATE
| Applicant | Scient'X, Round Rock TX, US |
| Decision | Substantially Equivalent, Sep 24, 2004 |
| Received | Aug 26, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042317
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.