ClearanceBrief
510(k) K051162 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

GENEROS SB SMALL BONE DISTRACTION IMPLANT

ApplicantOrthonetx, Inc., Superior CO, US
DecisionSubstantially Equivalent, Jul 19, 2005
ReceivedMay 5, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051162

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.