Cleared Traditional

Tigereye ST CTO-Crossing Catheter

K230594 · Avinger, Inc. · Cardiovascular

Apr 2023

Decision

53d

Days

Class 2

Risk

About This 510(k) Submission

K230594 is an FDA 510(k) clearance for the Tigereye ST CTO-Crossing Catheter, a Catheter For Crossing Total Occlusions (Class II — Special Controls, product code PDU), submitted by Avinger, Inc. (Redwood City, US). The FDA issued a Cleared decision on April 25, 2023, 53 days after receiving the submission on March 3, 2023. This device falls under the Cardiovascular review panel. Regulated under 21 CFR 870.1250.

Submission Details

510(k) Number	K230594 FDA.gov
FDA Decision	Cleared SESE
Date Received	March 03, 2023
Decision Date	April 25, 2023
Days to Decision	53 days
Submission Type	Traditional
Review Panel	Cardiovascular (CV)
Summary	Summary PDF

Device Classification

Product Code	PDU — Catheter For Crossing Total Occlusions
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 870.1250
Definition	To Facilitate The Intraluminal Placement Of Conventional Guidewires Beyond Stenotic Lesions (including Subchronic And Chronic Total Occlusions) In The Peripheral Vasculature Prior To Further Percutaneous Intervention, Such As Angioplasty, Atherectomy Or Stent Placement.