Cleared Traditional

K254174 - Surgical Power System

K254174 is an FDA 510(k) clearance for Surgical Power System, manufactured by Guizhou Zirui Technology Co., Ltd.. The device is a Class 2 Neurology device with product code HBC cleared through the Traditional 510(k) pathway after a 262-day FDA review.

K254174 · Guizhou Zirui Technology Co., Ltd. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2026
Decision
262d
Days
Class 2
Risk

K254174 is an FDA 510(k) clearance for the Surgical Power System. Classified as Motor, Drill, Electric (product code HBC), Class II - Special Controls.

Submitted by Guizhou Zirui Technology Co., Ltd. (Zunyi, CN). The FDA issued a Cleared decision on September 11, 2026 after a review of 262 days - an extended review cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4360 - the FDA neurology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Guizhou Zirui Technology Co., Ltd. devices

FDA 510(k) Submission Details - K254174

510(k) Number K254174 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 23, 2025
Decision Date September 11, 2026
Days to Decision 262 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
113d slower than avg
Panel avg: 149d · This submission: 262d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HBC Device Classification - Class 2, Special Controls

Product Code HBC Motor, Drill, Electric
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4360
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Neurology devices follow this clearance model.

Regulatory Consultant

Nanos Medical Shanghai Limited
Yoyo Chen

The regulatory consultant manages the 510(k) submission process on behalf of the applicant - coordinating technical documentation, predicate strategy and FDA communications. Identifying the consultant behind a submission is a key signal for competitive regulatory intelligence.

Regulatory Peers - HBC Motor, Drill, Electric

All 24
Devices cleared under the same product code (HBC) and FDA review panel - the closest regulatory comparables to K254174.
Traus SSG10 Surgical System
K233153 · Saeshin Precision Co., Ltd. · Sep 2024
Traus SSG30 Surgical System
K232938 · Saeshin Precision Co., Ltd. · Sep 2024
ORiGO System
K213697 · Bien-Air Surgery SA · Oct 2022
Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)
K220485 · The Anspach Effort, Inc. · May 2022
hekaDrill
K193630 · Zethon, Ltd. · Apr 2021
MR8 Drill System, Midas Rex MR8 ClearView Tools
K183515 · Medtronic Powered Surgical Solutions · May 2019