ClearanceBrief
510(k) K112069 ยท PHX Shoulder Prosthesis, Reverse Configuration

RSP GLENOID BASEPLATE POROUS COATED

ApplicantEncore Medical L.P., Austin TX, US
DecisionSubstantially Equivalent, Nov 15, 2011
ReceivedJul 20, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112069

DateFirm and productCodeLinked 510(k)
Dec 12, 2023Encore Medical, LP
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Open, Classified
PHXNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.