ClearanceBrief
510(k) K081586 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

REPROCESSED EXTERNAL FIXATION DEVICE

ApplicantSterilmed, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Aug 18, 2008
ReceivedJun 5, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K081586

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.