ClearanceBrief
510(k) K061863 ยท HWC Screw, Fixation, Bone

ARTHREX CORKSCREW SUTURE ANCHOR, TAK, AND PUSHLOCK FAMILY

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Oct 19, 2006
ReceivedJun 30, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061863

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.