510(k) K012634 ยท KTW Appliance, Fixation, Nail/Blade/Plate Combination, Single Component
REPROCESSED EXTERNAL FIXATION DEVICE
| Applicant | Alliance Medical, Inc., Phoenix AZ, US |
| Decision | Substantially Equivalent, Jun 24, 2002 |
| Received | Aug 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012634
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.