Solar Lumbar Interbody Fusion System— 510(k) K240326

Name: FDA 510(k) clearance K240326
Creator: U.S. Food and Drug Administration
Published: 2024-07-29

Substantially Equivalent

Degen Medical, Inc.

FDA 510(k) clearance K240326 for Solar Lumbar Interbody Fusion System, Substantially Equivalent on 2024-07-29. Applicant: Degen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Degen Medical, Inc.
Product code: Code MAX
Device class: Class 2
Regulation: 21 CFR 888.3080
Advisory panel: Orthopedic
Date received: 2024-02-02
Decision date: 2024-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Florence, SC, 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.