Preview Shoulder— 510(k) K210556

Substantially Equivalent

Genesis Software Innovations

FDA 510(k) clearance K210556 for Preview Shoulder, Substantially Equivalent on 2021-04-21. Applicant: Genesis Software Innovations. Device class: 2.

Clearance details

Applicant: Genesis Software Innovations
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2021-02-25
Decision date: 2021-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grand Rapids, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Genesis Software Innovations

K240172 — Preview Shoulder2024-04-04

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