510(k) K240678

ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUM 3DP Technology by Depuy Ireland UC — Product Code MBH

K240678 is an FDA 510(k) premarket notification submitted by Depuy Ireland UC for the device "ATTUNE® Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUM 3DP Technology". The FDA issued a decision of Substantially Equivalent on June 18, 2024. The device falls under product code MBH (Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer), a Class II device regulated under 21 CFR 888.3565. Depuy Ireland UC has at least 10 other 510(k) clearances on record.