Altus Spine Titanium Interbody Fusion System— 510(k) K170512

Substantially Equivalent

Altus Partners, LLC

FDA 510(k) clearance K170512 for Altus Spine Titanium Interbody Fusion System, Substantially Equivalent on 2017-03-10. Applicant: Altus Partners, LLC.

Clearance details

Applicant: Altus Partners, LLC
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2017-02-21
Decision date: 2017-03-10
Decision: Substantially Equivalent
Clearance type: Special
Location: West Chester, PA, US

Download summary PDF View on FDA.gov ↗

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.