ClearanceBrief
510(k) K260561 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue

Arthrex FiberTak Suture Anchor

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Mar 20, 2026
ReceivedFeb 19, 2026
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K260561

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.