Aurora® Anterior Lumbar Plate Sytstem— 510(k) K201079

Substantially Equivalent

Prism Surgical Design Pty , Ltd.

FDA 510(k) clearance K201079 for Aurora® Anterior Lumbar Plate Sytstem, Substantially Equivalent on 2020-08-05. Applicant: Prism Surgical Design Pty , Ltd..

Clearance details

Applicant: Prism Surgical Design Pty , Ltd.
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2020-04-22
Decision date: 2020-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milton, AU

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.