ABARIS— 510(k) K053610

Name: FDA 510(k) clearance K053610
Creator: U.S. Food and Drug Administration
Published: 2006-04-19

Substantially Equivalent

Traxtal Technologies, Inc.

FDA 510(k) clearance K053610 for ABARIS, Substantially Equivalent on 2006-04-19. Applicant: Traxtal Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Traxtal Technologies, Inc.
Product code: Code JAK
Device class: Class 2
Regulation: 21 CFR 892.1750
Advisory panel: Radiology
Date received: 2005-12-27
Decision date: 2006-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, Ontario, CA

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JAK

product code JAK

Death: 27
Injury: 571
Malfunction: 779
Total: 1,377

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.