ClearanceBrief
510(k) K220792 ยท MBF Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented

SMR Reverse Liner

ApplicantLima Corporate S.P.A., Villanova Di San Daniele Del Friuli, IT
DecisionSubstantially Equivalent, May 19, 2022
ReceivedMar 18, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220792

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.