ClearanceBrief
510(k) K231841 ยท OUR Sacroiliac Joint Fixation

PathLoc SI Joint Fusion System

ApplicantL&K BIOMED Co., Ltd., Yongin-Si, KR
DecisionSubstantially Equivalent, Jul 14, 2023
ReceivedJun 22, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K231841

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.