ClearanceBrief
510(k) K926232 ยท HSB Rod, Fixation, Intramedullary And Accessories

ALTA CFX ROD SYSTEM

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Jun 17, 1993
ReceivedDec 11, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926232

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.