K251969

Substantially Equivalent

Atlas Spine Project X Expandable Posterior Lumbar Interbody System

Applicant: Atlas Spine, Inc.
Product code: MAX
Advisory panel: Orthopedic
Date received: 2025-06-26
Decision date: 2025-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jupiter, FL, US

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.