ClearanceBrief
510(k) K021883 ยท HWC Screw, Fixation, Bone

BIOFASTIN RC THREADED SUTURE ANCHOR

ApplicantMitek Worldwide, Norwood MA, US
DecisionSubstantially Equivalent, Jul 1, 2002
ReceivedJun 7, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021883

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.