ClearanceBrief
510(k) K991971 ยท HTY Pin, Fixation, Smooth

ARTHREX CHONDRAL DART, MODEL AR-4005B-18

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Aug 4, 2000
ReceivedJun 11, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K991971

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.