ClearanceBrief
510(k) K980102 ยท HSB Rod, Fixation, Intramedullary And Accessories

BTI HUMERAL INTRAMEDULLARY ROD SYSTEM

ApplicantBiodynamic Technologies, Inc., Deerfield Beach FL, US
DecisionSubstantially Equivalent, Apr 3, 1998
ReceivedJan 12, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980102

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.