Integrity Spine Lumbar Interbody Fusion System— 510(k) K151819

Name: FDA 510(k) clearance K151819
Creator: U.S. Food and Drug Administration
Published: 2015-11-10

Substantially Equivalent

Integrity Spine Lumbar Interbody Fusion System

FDA 510(k) clearance K151819 for Integrity Spine Lumbar Interbody Fusion System, Substantially Equivalent on 2015-11-10. Applicant: Integrity Spine Lumbar Interbody Fusion System. Device class: 2.

Clearance details

Applicant: Integrity Spine Lumbar Interbody Fusion System
Product code: Code MAX
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2015-07-06
Decision date: 2015-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, 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.