EVOL Spinal Interbody System, EVOS Lumbar Interbody System— 510(k) K180891

Substantially Equivalent

Cutting Edge Spine, LLC

FDA 510(k) clearance K180891 for EVOL Spinal Interbody System, EVOS Lumbar Interbody System, Substantially Equivalent on 2018-05-04. Applicant: Cutting Edge Spine, LLC.

Clearance details

Applicant: Cutting Edge Spine, LLC
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2018-04-05
Decision date: 2018-05-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Waxhaw, NC, 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.