HEALIX ADVANCE KNOTLESS Anchor— 510(k) K171114

Name: FDA 510(k) clearance K171114
Creator: U.S. Food and Drug Administration
Published: 2017-11-27

Substantially Equivalent

Medos International SARL

FDA 510(k) clearance K171114 for HEALIX ADVANCE KNOTLESS Anchor, Substantially Equivalent on 2017-11-27. Applicant: Medos International SARL. Device class: 2.

Clearance details

Applicant: Medos International SARL
Product code: Code MAI
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 2017-04-14
Decision date: 2017-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Le Locle, CH

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MAI

product code MAI

Injury: 1,948
Malfunction: 8,580
Total: 10,528

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.