ARTHREX KNOTLESS SUTURETAK ANCHOR— 510(k) K120155

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K120155 for ARTHREX KNOTLESS SUTURETAK ANCHOR, Substantially Equivalent on 2012-02-17. Applicant: Arthrex, Inc..

Clearance details

Applicant: Arthrex, Inc.
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2012-01-18
Decision date: 2012-02-17
Decision: Substantially Equivalent
Clearance type: Special
Location: Naples, FL, US

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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.