Cannulated Screw and Kirschner (K wire) System— 510(k) K252758

Substantially Equivalent

Orthonovis, Inc.

FDA 510(k) clearance K252758 for Cannulated Screw and Kirschner (K wire) System, Substantially Equivalent on 2025-10-02. Applicant: Orthonovis, Inc..

Clearance details

Applicant: Orthonovis, Inc.
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 2025-08-29
Decision date: 2025-10-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Palm Coast, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.