ClearanceBrief
510(k) K925456 ยท HRX Arthroscope

ARTHROSCOPIC INSTRUMENTS

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Mar 4, 1993
ReceivedOct 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925456

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.