ABBOTT SPINE UNIVERSAL CLAMP SYSTEM— 510(k) K060009

Name: FDA 510(k) clearance K060009
Creator: U.S. Food and Drug Administration
Published: 2006-03-06

Substantially Equivalent

Abbott Spine, Inc.

FDA 510(k) clearance K060009 for ABBOTT SPINE UNIVERSAL CLAMP SYSTEM, Substantially Equivalent on 2006-03-06. Applicant: Abbott Spine, Inc.. Device class: 2.

Clearance details

Applicant: Abbott Spine, Inc.
Product code: Code JDQ
Device class: Class 2
Regulation: 21 CFR 888.3010
Advisory panel: Orthopedic
Date received: 2006-01-03
Decision date: 2006-03-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code JDQ

product code JDQ

Death: 9
Injury: 330
Total: 339

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.