Catamaran SI Joint Fusion System— 510(k) K250403

Substantially Equivalent

Tenon Medical

FDA 510(k) clearance K250403 for Catamaran SI Joint Fusion System, Substantially Equivalent on 2025-03-21. Applicant: Tenon Medical.

Clearance details

Applicant: Tenon Medical
Product code: Code OUR
Advisory panel: Orthopedic
Date received: 2025-02-12
Decision date: 2025-03-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Los Gatos, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OUR

product code OUR

Death: 3
Injury: 347
Total: 350

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.