SPINAUT-V, SPINAUT-S, SPINAUT-I— 510(k) K151268

Substantially Equivalent

Imedicom Co., Ltd.

FDA 510(k) clearance K151268 for SPINAUT-V, SPINAUT-S, SPINAUT-I, Substantially Equivalent on 2016-03-16. Applicant: Imedicom Co., Ltd..

Clearance details

Applicant: Imedicom Co., Ltd.
Product code: Code HRX
Advisory panel: Orthopedic
Date received: 2015-05-13
Decision date: 2016-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gunpo-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRX

product code HRX

Injury: 623
Malfunction: 11,257
Total: 11,880

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.