Juliet Ti— 510(k) K181203

Substantially Equivalent

Spineart

FDA 510(k) clearance K181203 for Juliet Ti, Substantially Equivalent on 2018-06-28. Applicant: Spineart.

Clearance details

Applicant: Spineart
Product code: Code MAX
Advisory panel: Orthopedic
Date received: 2018-05-07
Decision date: 2018-06-28
Decision: Substantially Equivalent
Clearance type: Special
Location: Plan Les Ouates, CH

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.