ClearanceBrief
510(k) K222007 ยท QHE Shoulder Arthroplasty Implantation System

Arthrex Virtual Implant Positioning (VIP) System

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, Mar 8, 2023
ReceivedJul 7, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222007

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.