510(k) K052918 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
REPROCESSED EXTERNAL FIXATION DEVICES
| Applicant | Alliance Medical Corp., Phoenix AZ, US |
| Decision | Substantially Equivalent, Jan 27, 2006 |
| Received | Oct 17, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052918
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.