ClearanceBrief
510(k) K100532 ยท HWC Screw, Fixation, Bone

VERSALOK PEEK ANCHOR WITH ORTHOCORD SUTURE, MODELS 210818, 210819

ApplicantDepuy Mitek, A Johnson & Johnson Company, Raynham MA, US
DecisionSubstantially Equivalent, Mar 17, 2010
ReceivedFeb 25, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K100532

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.