OSSIOfiber® Interference Screw— 510(k) K252022

Substantially Equivalent

OSSIO , Ltd.

FDA 510(k) clearance K252022 for OSSIOfiber® Interference Screw, Substantially Equivalent on 2025-08-19. Applicant: OSSIO , Ltd..

Clearance details

Applicant: OSSIO , Ltd.
Product code: Code MAI
Advisory panel: Orthopedic
Date received: 2025-06-30
Decision date: 2025-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Caesarea, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code MAI

product code MAI

Injury: 1,948
Malfunction: 8,580
Total: 10,528

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.