K162220

Substantially Equivalent

DIO Medical IVA (ACIF, DLIF, PLIF, TLIF,and ALIF) Cage

Applicant: Dio Medical Co., Ltd.
Product 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

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.