LIFE SPINE FACET SCREW SPINAL SYSTEM— 510(k) K090865

Name: FDA 510(k) clearance K090865
Creator: U.S. Food and Drug Administration
Published: 2009-06-26

Substantially Equivalent

Life Spine

FDA 510(k) clearance K090865 for LIFE SPINE FACET SCREW SPINAL SYSTEM, Substantially Equivalent on 2009-06-26. Applicant: Life Spine. Device class: Unclassified.

Clearance details

Applicant: Life Spine
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2009-03-30
Decision date: 2009-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
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.