ClearanceBrief
510(k) K230904 ยท QHE Shoulder Arthroplasty Implantation System

Arthrex Virtual Implant Positioning (VIP) System

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Jun 22, 2023
ReceivedMar 31, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230904

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.