Rattlesnake

64 catalogue numbers from RS6116, 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
64catalogue 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 Rattlesnake
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 2017-02-09
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
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Rattlesnake
Catalogue number Size Status
RS6116 In distribution
RS7016 In distribution
RS7110 In distribution
RS7208 In distribution
RS7014 In distribution
RS8514 In distribution
RS8016 In distribution
RS7610 In distribution
RS6012 In distribution
RS8112 In distribution
RS8014 In distribution
RS7116 In distribution
RS6210 In distribution
RS6008 In distribution
RS7514 In distribution
RS6112 In distribution
RS8516 In distribution
RS7512 In distribution
RS7112 In distribution
RS6610 In distribution
RS6512 In distribution
RS6616 In distribution
RS6508 In distribution
RS7212 In distribution
RS7508 In distribution
RS6010 In distribution
RS8510 In distribution
RS6514 In distribution
RS6612 In distribution
RS8110 In distribution
RS8610 In distribution
RS8012 In distribution
RS7210 In distribution
RS7214 In distribution
RS8010 In distribution
RS7516 In distribution
RS6614 In distribution
RS6216 In distribution
RS8008 In distribution
RS7510 In distribution
RS6014 In distribution
RS6212 In distribution
RS7010 In distribution
RS7012 In distribution
RS7114 In distribution
RS6510 In distribution
RS7616 In distribution
RS7612 In distribution
RS7008 In distribution
RS6114 In distribution
RS8616 In distribution
RS8116 In distribution
RS8614 In distribution
RS7216 In distribution
RS8512 In distribution
RS6110 In distribution
RS8114 In distribution
RS6016 In distribution
RS7614 In distribution
RS8612 In distribution
RS8508 In distribution
RS6516 In distribution
RS6214 In distribution
RS6208 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 Rattlesnake
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