ClearanceBrief
510(k) K012923 ยท GAT Suture, Nonabsorbable, Synthetic, Polyethylene

ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Oct 4, 2001
ReceivedAug 31, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012923

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.