Life Spine Laminoplasty System— 510(k) K181717

Name: FDA 510(k) clearance K181717
Creator: U.S. Food and Drug Administration
Published: 2018-10-12

Substantially Equivalent

Life Spine, Inc.

FDA 510(k) clearance K181717 for Life Spine Laminoplasty System, Substantially Equivalent on 2018-10-12. Applicant: Life Spine, Inc.. Device class: 2.

Clearance details

Applicant: Life Spine, Inc.
Product code: Code NQW
Device class: Class 2
Regulation: 21 CFR 888.3050
Advisory panel: Orthopedic
Date received: 2018-06-28
Decision date: 2018-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Huntley, 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.