ANKLE INSTRUMENTS (FREEMAN-SWANSON)— 510(k) K761021

Name: FDA 510(k) clearance K761021
Creator: U.S. Food and Drug Administration
Published: 1976-11-23

Substantially Equivalent

Medishield, Inc.

FDA 510(k) clearance K761021 for ANKLE INSTRUMENTS (FREEMAN-SWANSON), Substantially Equivalent on 1976-11-23. Applicant: Medishield, Inc.. Device class: 2.

Clearance details

Applicant: Medishield, Inc.
Product code: Code HSN
Device class: Class 2
Regulation: 21 CFR 888.3110
Advisory panel: Orthopedic
Date received: 1976-11-11
Decision date: 1976-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HSN

product code HSN

Death: 3
Injury: 4,711
Total: 4,714

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.