Arthrex 2.4mm Knotless Hip SutureTak® Suture Anchor— 510(k) K232340

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K232340 for Arthrex 2.4mm Knotless Hip SutureTak® Suture Anchor, Substantially Equivalent on 2023-09-01. Applicant: Arthrex, Inc..

Clearance details

Applicant: Arthrex, Inc.
Product code: Code MBI
Advisory panel: Orthopedic
Date received: 2023-08-04
Decision date: 2023-09-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Naples, FL, 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.