COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE— 510(k) K082535

Name: FDA 510(k) clearance K082535
Creator: U.S. Food and Drug Administration
Published: 2008-12-01

Substantially Equivalent

Surgical Devices, A Global Business Unit Covidien

FDA 510(k) clearance K082535 for COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE, Substantially Equivalent on 2008-12-01. Applicant: Surgical Devices, A Global Business Unit Covidien. Device class: 2.

Clearance details

Applicant: Surgical Devices, A Global Business Unit Covidien
Product code: Code GAT
Device class: Class 2
Regulation: 21 CFR 878.5000
Advisory panel: General, Plastic Surgery
Date received: 2008-09-02
Decision date: 2008-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Haven, CT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GAT

product code GAT

Death: 19
Injury: 4,163
Malfunction: 8,646
Other: 2
Total: 12,830

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.