ClearanceBrief
510(k) K860356 ยท LYS Bone Mill

ORTHOBLEND POWERED BONE MILL

ApplicantZimmer, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 8, 1986
ReceivedJan 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860356

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.