ClearanceBrief
510(k) K926062 ยท HRX Arthroscope

ARTHROSCOPIC KNEE INSTRUMENTS

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Mar 16, 1993
ReceivedDec 1, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926062

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.