VERTICALE® Posterior Spinal Fixation System/VERTICALE® System— 510(k) K171421

Substantially Equivalent

Silony Medical GmbH

FDA 510(k) clearance K171421 for VERTICALE® Posterior Spinal Fixation System/VERTICALE® System, Substantially Equivalent on 2018-01-10. Applicant: Silony Medical GmbH.

Clearance details

Applicant: Silony Medical GmbH
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2017-05-15
Decision date: 2018-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leinfelden-Echterdingen, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code NKB

product code NKB

Death: 27
Injury: 5,033
Malfunction: 4,140
Total: 9,200

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.