ClearanceBrief
510(k) K243173 ยท OYK Ankle Arthroplasty Implantation System

Salto Talaris Ankle PSI System

Applicant3D Systems, Inc., Littleton CO, US
DecisionSubstantially Equivalent, Oct 25, 2024
ReceivedSep 30, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K243173

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.