ClearanceBrief
510(k) K043337 ยท HWC Screw, Fixation, Bone

ARTHREX BIO-CORKSCREW FT SUTURE ANCHOR

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Dec 14, 2004
ReceivedDec 3, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K043337

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.