ScanDiags Ortho L-Spine MR-Q— 510(k) K242607

Substantially Equivalent

Scandiags AG

FDA 510(k) clearance K242607 for ScanDiags Ortho L-Spine MR-Q, Substantially Equivalent on 2025-02-21. Applicant: Scandiags AG. Device class: 2.

Clearance details

Applicant: Scandiags AG
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2024-09-03
Decision date: 2025-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallisellen, CH

Download summary PDF View on FDA.gov ↗

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