ClearanceBrief
510(k) K841619 ยท FZX Guide, Surgical, Instrument

DRILL GUIDE

ApplicantPlastafil, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 11, 1984
ReceivedApr 19, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841619

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.