TRYPTIK2C-plate Anterior Cervical Plate System— 510(k) K153042

Substantially Equivalent

Spineart

FDA 510(k) clearance K153042 for TRYPTIK2C-plate Anterior Cervical Plate System, Substantially Equivalent on 2016-03-28. Applicant: Spineart.

Clearance details

Applicant: Spineart
Product code: Code KWQ
Advisory panel: Orthopedic
Date received: 2015-10-19
Decision date: 2016-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geneva, CH

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.