VUSION CS PLUS— 510(k) K122588

Name: FDA 510(k) clearance K122588
Creator: U.S. Food and Drug Administration
Published: 2013-06-12

Substantially Equivalent

Ortho Development Corp.

FDA 510(k) clearance K122588 for VUSION CS PLUS, Substantially Equivalent on 2013-06-12. Applicant: Ortho Development Corp.. Device class: 2.

Clearance details

Applicant: Ortho Development Corp.
Product code: Code ODP
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2012-08-24
Decision date: 2013-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Draper, UT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.