Axis Anterior Cervical Plate System— 510(k) K173867

Substantially Equivalent

Axis Orthopaedics

FDA 510(k) clearance K173867 for Axis Anterior Cervical Plate System, Substantially Equivalent on 2018-04-05. Applicant: Axis Orthopaedics.

Clearance details

Applicant: Axis Orthopaedics
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2017-12-20
Decision date: 2018-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Soldotna, AK, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KWQ

product code KWQ

Death: 8
Injury: 1,212
Malfunction: 1,233
Total: 2,453

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.