EZ SPLINT & EZ SPLINT PM— 510(k) K022809

Name: FDA 510(k) clearance K022809
Creator: U.S. Food and Drug Administration
Published: 2003-10-17

Substantially Equivalent

Power Products, Inc.-Splintek

FDA 510(k) clearance K022809 for EZ SPLINT & EZ SPLINT PM, Substantially Equivalent on 2003-10-17. Applicant: Power Products, Inc.-Splintek. Device class: Unclassified.

Clearance details

Applicant: Power Products, Inc.-Splintek
Product code: Code MQC
Device class: Unclassified
Advisory panel: Unknown
Date received: 2002-08-23
Decision date: 2003-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MQC

product code MQC

Injury: 377
Total: 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.