Reliance Interspinous Plate System— 510(k) K142217

Name: FDA 510(k) clearance K142217
Creator: U.S. Food and Drug Administration
Published: 2015-04-02

Substantially Equivalent

Reliance Medical Systems, LLC

FDA 510(k) clearance K142217 for Reliance Interspinous Plate System, Substantially Equivalent on 2015-04-02. Applicant: Reliance Medical Systems, LLC. Device class: 2.

Clearance details

Applicant: Reliance Medical Systems, LLC
Product code: Product code PEK
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2014-08-12
Decision date: 2015-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bountiful, UT, US

Download summary PDF View on FDA.gov ↗

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