ArthroTAK Tendon Anchor Kit— 510(k) K252635

Substantially Equivalent

ArthroTAK, LLC

FDA 510(k) clearance K252635 for ArthroTAK Tendon Anchor Kit, Substantially Equivalent on 2026-05-01. Applicant: ArthroTAK, LLC.

Clearance details

Applicant: ArthroTAK, LLC
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2025-08-20
Decision date: 2026-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Missoula, MT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MBI

product code MBI

Injury: 3,163
Malfunction: 13,006
Other: 2
Total: 16,171

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.