510(k) K031772 ยท KWP Appliance, Fixation, Spinal Interlaminal
TI FENESTRATED PLATE
| Applicant | Interpore Cross Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 5, 2003 |
| Received | Jun 9, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K031772
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.