MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR— 510(k) K061698

Name: FDA 510(k) clearance K061698
Creator: U.S. Food and Drug Administration
Published: 2006-07-12

Substantially Equivalent

Life Spine

FDA 510(k) clearance K061698 for MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR, Substantially Equivalent on 2006-07-12. Applicant: Life Spine. Device class: 2.

Clearance details

Applicant: Life Spine
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2006-06-16
Decision date: 2006-07-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Hoffman Estates, IL, 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.