INION CPS 2.5/2.8 SCREW— 510(k) K022981

Name: FDA 510(k) clearance K022981
Creator: U.S. Food and Drug Administration
Published: 2002-09-12

Substantially Equivalent

Inion , Ltd.

FDA 510(k) clearance K022981 for INION CPS 2.5/2.8 SCREW, Substantially Equivalent on 2002-09-12. Applicant: Inion , Ltd.. Device class: 2.

Clearance details

Applicant: Inion , Ltd.
Product code: Code HWC
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 2002-09-09
Decision date: 2002-09-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Tampere, FI

Download summary PDF View on FDA.gov ↗

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K060393 — INION HEXALON BIODEGRADABLE ACL/PCL SCREW2006-03-13
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Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.