LumiVy Lumbar IBF System— 510(k) K223412

Name: FDA 510(k) clearance K223412
Creator: U.S. Food and Drug Administration
Published: 2023-01-06

Substantially Equivalent

Vy Spine, LLC

FDA 510(k) clearance K223412 for LumiVy Lumbar IBF System, Substantially Equivalent on 2023-01-06. Applicant: Vy Spine, LLC. Device class: 2.

Clearance details

Applicant: Vy Spine, LLC
Product code: Code MAX
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2022-11-09
Decision date: 2023-01-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Tallahassee, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MAX

product code MAX

Death: 13
Injury: 1,305
Malfunction: 2,885
Total: 4,203

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.