ClearanceBrief
510(k) K202569 ยท HWC Screw, Fixation, Bone

Responsive Arthroscopy Interference Screw System

ApplicantResponsive Arthroscopy, LLC, Minneapolis MN, US
DecisionSubstantially Equivalent, Sep 23, 2020
ReceivedSep 4, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K202569

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.