TIGER SPINE SYSTEM— 510(k) K120696

Name: FDA 510(k) clearance K120696
Creator: U.S. Food and Drug Administration
Published: 2012-04-02

Substantially Equivalent

Corelink, LLC

FDA 510(k) clearance K120696 for TIGER SPINE SYSTEM, Substantially Equivalent on 2012-04-02. Applicant: Corelink, LLC. Device class: 2.

Clearance details

Applicant: Corelink, LLC
Product code: Code MNI
Device class: Class 2
Regulation: 21 CFR 888.3070
Advisory panel: Orthopedic
Date received: 2012-03-07
Decision date: 2012-04-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Round Rock, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.