REXIOUS SPINAL FIXATION SYSTEM— 510(k) K111362

Substantially Equivalent

Dio Medical Co., Ltd.

FDA 510(k) clearance K111362 for REXIOUS SPINAL FIXATION SYSTEM, Substantially Equivalent on 2011-07-21. Applicant: Dio Medical Co., Ltd..

Clearance details

Applicant: Dio Medical Co., Ltd.
Product code: Code MNH
Advisory panel: Orthopedic
Date received: 2011-05-16
Decision date: 2011-07-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Brea, CA, US

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Adverse events under product code MNH

product code MNH

Injury: 978
Malfunction: 793
Total: 1,771

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.