ClearanceBrief
510(k) K023851 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

PRECIMED HIP SCREW SYSTEM

ApplicantPrecimed, Inc., Chester Springs PA, US
DecisionSubstantially Equivalent, Jan 28, 2003
ReceivedNov 19, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023851

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.