Corus™ Spinal System

The CORUS Spinal System is a set of instruments for posterior cervical fusion in patients with cervical degenerative disc disease. The instruments provide access to the back of the cervical…

Registry build 21.09.26

The CORUS Spinal System is a set of instruments for posterior cervical fusion in patients with cervical degenerative disc disease. The instruments provide access to the back of the cervical spine and prepare bone surfaces at the lateral masses and facet joints for graft placement.

Preparation involves decortication, removing surface bone before autograft or allograft is applied. The set combines access tools with instruments for this bone preparation and graft placement. Its role is to perform these surgical steps as part of a fusion procedure.

Listed Item

The CORUS Spinal System instruments are used to access and prepare the posterior cervical spine for joint fusion by decortication of bone surfaces, including the posterior lateral mass and facet joints, combined with application of allograft or autograft in patients with or without anterior or posterior instrumentation. It is recommended that commercially available autograft or allograft be used to aid fusion. Autograft or allograft material is not supplied as part of the system.

Instrument Set

The system includes an access chisel and handle, guide tube, trephine, rasp, burr, bone graft tamp and fork mallet. The instruments are supplied sterile and are intended for a single use.

21manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (7), Jiangsu (6), Guangdong (5). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HRX
Manufacturer City Province Registered as Device types
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Sanmina Kunshan Jiangsu Contract manufacturer 15
Peter’s Technology (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 9
Jiangsu Shenli Medical Production Co., Ltd. Changzhou Jiangsu Contract manufacturer 6
PAN-International Precision Electronic Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Arthrex (Shanghai) Co., Ltd. Shanghai Shanghai Exporter 38
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26

Showing 12 of 21. All 21 manufacturers in China registered for Arthroscope

Record

Regulatory record for Corus™ Spinal System
Listed by Providence Medical Technology, Inc., United States
FDA product code HRX
Device type Arthroscope
Device class Class 2
Regulation 21 CFR 888.1100
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K190201
Record published 2019-07-23
Record revised 2025-07-10 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Corus™ Spinal System
Catalogue number Size Status
DX-22-100 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Surgical Direct Surgical Direct, Inc. 299
Arthroscope Karl Storz GmbH & Co. KG 278
Conmed/Linvatec Provision 265
Arthroscope Smith & Nephew, Inc. 255
Medline Medline Industries, Inc. 205
Arthroscope Sterilmed, Inc. 184
Sustainable Technologies Provision 150
Medline Renewal Medline Industries, Inc. 123
Stryker Provision 113
Arthrex® Arthrex, Inc. 109
Arthrex Provision 109
Eberle Eberle GmbH & Co. KG 92

Showing 12 of 567. All products under Arthroscope

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212636 2021-10-15
K190201 2019-03-08
K180876 2018-05-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer