DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage— 510(k) K162220

Substantially Equivalent

Dio Medical Co., Ltd.

FDA 510(k) clearance K162220 for DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage, Substantially Equivalent on 2016-11-21. Applicant: Dio Medical Co., Ltd..

Clearance details

Applicant: Dio Medical Co., Ltd.
Product code: Code ODP
Advisory panel: Orthopedic
Date received: 2016-08-08
Decision date: 2016-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sagimakgol-Ro Jungwon-Gu Seongnam-Si, KR

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.