ClearanceBrief
510(k) K910483 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

MONOTUBE EXTERNAL FIXATION SYSTEM

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Jul 14, 1992
ReceivedFeb 6, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910483

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.