ClearanceBrief
510(k) K190588 ยท PHX Shoulder Prosthesis, Reverse Configuration

Integra TITAN Reverse Shoulder System

ApplicantIntegra LifeSciences Corporation, Austin TX, US
DecisionSubstantially Equivalent, Dec 2, 2019
ReceivedMar 7, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190588

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.