510(k) K023714 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
REPROCESSED EXTERNAL FIXATION DEVICE
| Applicant | Alliance Medical Corp., Phoenix AZ, US |
| Decision | Substantially Equivalent, Feb 3, 2003 |
| Received | Nov 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023714
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.