Premier— 510(k) K160320

Substantially Equivalent

Shandong Weigao Orthopaedic Device Co., Ltd.

FDA 510(k) clearance K160320 for Premier, Substantially Equivalent on 2016-04-01. Applicant: Shandong Weigao Orthopaedic Device Co., Ltd..

Clearance details

Applicant: Shandong Weigao Orthopaedic Device Co., Ltd.
Product code: Code MNI
Advisory panel: Orthopedic
Date received: 2016-02-05
Decision date: 2016-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weihai, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.