Curiteva Pedicle Screw System— 510(k) K191810

Substantially Equivalent

Curiteva, Inc.

FDA 510(k) clearance K191810 for Curiteva Pedicle Screw System, Substantially Equivalent on 2019-08-28. Applicant: Curiteva, Inc..

Clearance details

Applicant: Curiteva, Inc.
Product code: Code NKB
Advisory panel: Orthopedic
Date received: 2019-07-05
Decision date: 2019-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tanner, AL, US

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.