zLOCK Lumbar Facet Fixation System— 510(k) K240085

Name: FDA 510(k) clearance K240085
Creator: U.S. Food and Drug Administration
Published: 2024-04-18

Substantially Equivalent

Zygofix , Ltd.

FDA 510(k) clearance K240085 for zLOCK Lumbar Facet Fixation System, Substantially Equivalent on 2024-04-18. Applicant: Zygofix , Ltd.. Device class: Unclassified.

Clearance details

Applicant: Zygofix , Ltd.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2024-01-11
Decision date: 2024-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Misgav, IL

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.