Curiteva Porous PEEK Cervical Interbody Fusion System— 510(k) K213030

Substantially Equivalent

Curiteva, Inc.

FDA 510(k) clearance K213030 for Curiteva Porous PEEK Cervical Interbody Fusion System, Substantially Equivalent on 2023-02-13. Applicant: Curiteva, Inc..

Clearance details

Applicant: Curiteva, Inc.
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2021-09-21
Decision date: 2023-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tanner, AL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.