SpineKure Kyphoplasty System— 510(k) K172871

Substantially Equivalent

Hanchang Co., Ltd.

FDA 510(k) clearance K172871 for SpineKure Kyphoplasty System, Substantially Equivalent on 2018-05-29. Applicant: Hanchang Co., Ltd..

Clearance details

Applicant: Hanchang Co., Ltd.
Product code: Code NDN
Advisory panel: Orthopedic
Date received: 2017-09-21
Decision date: 2018-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bucheon-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code NDN

product code NDN

Death: 24
Injury: 407
Malfunction: 1,975
Total: 2,406

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.