510(k) K083789 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
ACE FISCHER EXTERNAL FIXATION SYSTEM
| Applicant | DePuy Orthopaedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Mar 23, 2009 |
| Received | Dec 19, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083789
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.