510(k) K023360 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
LEFORTE SYSTEM BONE PLATE
| Applicant | Jeil Medical Corporation, Deer Field IL, US |
| Decision | Substantially Equivalent, Oct 25, 2002 |
| Received | Oct 7, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023360
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.