510(k) K260223

Aristotle Mini Guidewire by Scientia Vascular, Inc. — Product Code MOF

K260223 is an FDA 510(k) premarket notification submitted by Scientia Vascular, Inc. for the device "Aristotle Mini Guidewire". The FDA issued a decision of Substantially Equivalent on August 6, 2026. The device falls under product code MOF (Guide, Wire, Catheter, Neurovasculature), a Class II device regulated under 21 CFR 870.1330. Scientia Vascular, Inc. has at least 10 other 510(k) clearances on record.