Arsenal Deformity Spinal Fixation System

Extended Body Monoaxial Screw, 6.0mm X 55mm

Registry build 21.09.26
13manufacturers in China registered for this device type
20catalogue numbers in this listing
3510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNH
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Changzhou Yonghua Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 8
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7

Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spondylolisthesis Spinal Fixation

Record

Regulatory record for Arsenal Deformity Spinal Fixation System
Listed by Alphatec Spine, Inc., United States
FDA product code MNH
Device type Orthosis, Spondylolisthesis Spinal Fixation
Device class Class 2
Regulation 21 CFR 888.3070
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K152968
Record published 2016-04-27
Record revised 2025-02-12 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 16 to 105 mm; outer diameter 3.5 to 10.5 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Arsenal Deformity Spinal Fixation System
Catalogue number Size Status
48001-35-24 Length 24 mm In distribution
47016-32 Length 32 mm In distribution
48900-075-105 Outer Diameter 7.5 mm In distribution
48027-55-070 Length 70 mm In distribution
48001-040-28 Outer Diameter 4 mm In distribution
48001-045-16 Length 16 mm In distribution
48027-55-080 Length 80 mm In distribution
48001-040-16 Outer Diameter 4 mm In distribution
48300-050-035 Length 35 mm In distribution
48027-55-075 Outer Diameter 5.5 mm In distribution
48001-35-16 Outer Diameter 3.5 mm In distribution
48027-55-085 Length 85 mm In distribution
48027-55-045 Length 45 mm In distribution
48001-040-24 Outer Diameter 4 mm In distribution
48200-060-055 Outer Diameter 6 mm In distribution
48200-065-035 Outer Diameter 6.5 mm In distribution
48700-000-105-035 Outer Diameter 10.5 mm In distribution
48200-070-070 Length 70 mm In distribution
48001-045-20 Length 20 mm In distribution
48027-55-035 Length 35 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 3,144
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 2,177
ReLine Nuvasive, Inc. 2,010
Creo Globus Medical, Inc. 1,619
Perfix™ Spinal System CG MedTech Co., Ltd. 1,476
Apex Spine System Spinecraft LLC 1,193
Olympic Astura Medical 1,173
Arsenal Alphatec Spine, Inc. 1,001
Revere Globus Medical, Inc. 997
Astra Spine System Spinecraft LLC 798
Apex-DL Spine System Spinecraft LLC 735
Zenius Spinal System Medyssey Co., Ltd. 712

Showing 12 of 811. All products under Orthosis, Spondylolisthesis Spinal Fixation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K090228 2009-04-29
K071890 2007-11-09
K061321 2006-07-07

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2012-09-25 Class II Nonconforming Material/Component The firm initiated the recall because the stainless steel guide-wire of the
Illico MIS Fixation System did not completely fit/pass through the tip of certain Illico Ti
Cannulated Polyaxial Screws, therefore rendering such screws nonfunction
209 screws 2013-03-29

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