510(k) K231954

Aristotle 18 Guidewire; Aristotle 24 Guidewire by Scientia Vascular, Inc. — Product Code MOF

K231954 is an FDA 510(k) premarket notification submitted by Scientia Vascular, Inc. for the device "Aristotle 18 Guidewire; Aristotle 24 Guidewire". The FDA issued a decision of Substantially Equivalent on August 1, 2023. 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.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 2023
Date Received
July 3, 2023
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Guide, Wire, Catheter, Neurovasculature
Device Class
Class II
Regulation Number
870.1330
Review Panel
NE
Submission Type