510(k) K110426 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
DYNA-EXTOR II
| Applicant | Bk Meditech, Co., Ltd., Stillwater MN, US |
| Decision | Substantially Equivalent, Nov 2, 2011 |
| Received | Feb 14, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110426
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.