510(k) K083636 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
REPROCESSED EXTERNAL FIXATION DEVICE
| Applicant | Sterilmed, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Mar 2, 2009 |
| Received | Dec 9, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083636
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.