510(k) K013823 ยท KWP Appliance, Fixation, Spinal Interlaminal
XIA SPINAL SYSTEM
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Dec 19, 2001 |
| Received | Nov 19, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013823
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.