Copperhead

65 catalogue numbers from C4010, listed by Eminent Spine, United States, under Spinal Vertebral Body Replacement Device. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
65catalogue numbers in this listing

Who Else Makes It

Concentrated in Shanghai (1), Jiangsu (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MQP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Copperhead
Listed by Eminent Spine, United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
510(k) K090064
Record published 2017-02-08
Record revised 2020-02-24 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Copperhead
Catalogue number Size Status
C4010 In distribution
C4107 In distribution
C5009 In distribution
C4108 In distribution
C6109 In distribution
C7109 In distribution
C4008 In distribution
C7009 In distribution
C7111 In distribution
C5110 In distribution
C4007 In distribution
C6111 In distribution
C4009 In distribution
C3110 In distribution
C4111 In distribution
C3007 In distribution
C3105 In distribution
C7008 In distribution
C7006 In distribution
C6112 In distribution
C7007 In distribution
C5108 In distribution
C6108 In distribution
C6007 In distribution
C4012 In distribution
C3111 In distribution
C7005 In distribution
C7112 In distribution
C6011 In distribution
C5007 In distribution
C4112 In distribution
C5109 In distribution
C6009 In distribution
C5008 In distribution
C3005 In distribution
C7012 In distribution
C5010 In distribution
C3011 In distribution
C3106 In distribution
C5006 In distribution
C7010 In distribution
C7110 In distribution
C7105 In distribution
C4011 In distribution
C3006 In distribution
C3108 In distribution
C3010 In distribution
C4109 In distribution
C5106 In distribution
C3107 In distribution
C7108 In distribution
C5107 In distribution
C6008 In distribution
C3109 In distribution
C6012 In distribution
C5111 In distribution
C7106 In distribution
C3009 In distribution
C6110 In distribution
C5011 In distribution
C4110 In distribution
C7011 In distribution
C3008 In distribution
C7107 In distribution
C6107 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 1,514
Capri™ Corpectomy Cage System VB Spine LLC 1,509
Aleutian® Interbody Systems VB Spine LLC 1,189
Fortify Globus Medical, Inc. 866
Matrixx System Nexxt Spine LLC 748
Ascend Alphatec Spine, Inc. 555
Zavation VBR Trial Zavation 548
Verte-Stack® Spinal System Medtronic Sofamor Danek, Inc. 484
Timberline® Lateral Interbody Fusion System Biomet Spine 470
Timberline Lateral Fusion System Biomet Spine 459
Novel Alphatec Spine, Inc. 447
Hawkeye™ Vertebral Body Replacement (VBR) Choice Spine, LP 368

Showing 12 of 683. All products under Spinal Vertebral Body Replacement Device

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Copperhead
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Spinal Solutions, LLC 510(k) number 2013-02-20 Class II Labeling design The recall of the Loaner Bin and Sterilization Trays for implants and instruments was initiated by Spinal Solutions because the directions for use and surgical techniques were not being provided to every physician and for every surgery. 24 units 2014-03-26

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