510(k) K234062

APTUS Hand Scaphoid Plates by Medartis AG — Product Code HRS

K234062 is an FDA 510(k) premarket notification submitted by Medartis AG for the device "APTUS Hand Scaphoid Plates". The FDA issued a decision of Substantially Equivalent on March 21, 2024. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Medartis AG has at least 10 other 510(k) clearances on record.