Hintermann Series H2 Total Ankle System— 510(k) K171004

Substantially Equivalent

Dt Medtech, LLC

FDA 510(k) clearance K171004 for Hintermann Series H2 Total Ankle System, Substantially Equivalent on 2017-11-07. Applicant: Dt Medtech, LLC.

Clearance details

Applicant: Dt Medtech, LLC
Product code: Code HSN
Advisory panel: Orthopedic
Date received: 2017-04-04
Decision date: 2017-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Towson, MD, US

Download summary PDF View on FDA.gov ↗

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.