ClearanceBrief
510(k) K892904 ยท HXY Brace, Drill

MITEK DRILL GUIDE

ApplicantMitek Surgical Products, Inc., Dedham MA, US
DecisionSubstantially Equivalent, Sep 28, 1989
ReceivedApr 20, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K892904

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.