ClearanceBrief
510(k) K220765 ยท JDQ Cerclage, Fixation

HS Fiber Cerclage

ApplicantRiverpoint Medical, LLC, Portland OR, US
DecisionSubstantially Equivalent, Jul 26, 2023
ReceivedMar 16, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220765

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.