510(k) K062513 ยท KWP Appliance, Fixation, Spinal Interlaminal
APEX SPINE SYSTEM
| Applicant | Spinecraft, Inc., Westchester IL, US |
| Decision | Substantially Equivalent, Dec 22, 2006 |
| Received | Aug 28, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062513
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.