SpineJack Expansion Kit— 510(k) K181262

Substantially Equivalent

Vexim SA

FDA 510(k) clearance K181262 for SpineJack Expansion Kit, Substantially Equivalent on 2018-08-30. Applicant: Vexim SA.

Clearance details

Applicant: Vexim SA
Product code: Code NDN
Advisory panel: Orthopedic
Date received: 2018-05-11
Decision date: 2018-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Balma, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code NDN

product code NDN

Death: 24
Injury: 407
Malfunction: 1,975
Total: 2,406

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.