ATLAS SPINAL CAGE, MODELS SC-150-007, 009, 011, 013, 015, 017.— 510(k) K060916

Name: FDA 510(k) clearance K060916
Creator: U.S. Food and Drug Administration
Published: 2006-06-08

Substantially Equivalent

Spinal Edge, LLC

FDA 510(k) clearance K060916 for ATLAS SPINAL CAGE, MODELS SC-150-007, 009, 011, 013, 015, 017., Substantially Equivalent on 2006-06-08. Applicant: Spinal Edge, LLC. Device class: 2.

Clearance details

Applicant: Spinal Edge, LLC
Product code: Code MQP
Device class: Class 2
Regulation: 21 CFR 888.3060
Advisory panel: Orthopedic
Date received: 2006-04-04
Decision date: 2006-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Westlake, OH, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

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.