icotec Interbody Cage System— 510(k) K172480

Substantially Equivalent

Icotec AG

FDA 510(k) clearance K172480 for icotec Interbody Cage System, Substantially Equivalent on 2018-05-17. Applicant: Icotec AG.

Clearance details

Applicant: Icotec AG
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2017-08-16
Decision date: 2018-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 9450 Altstaetten (Sg), CH

Download summary PDF View on FDA.gov ↗

Adverse events under product code ODP

product code ODP

Injury: 310
Total: 310

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.