ROI-C

ROI-C Implant 12X15.5 H8

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
8510(k) clearances naming this product code

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 ROI-C
Listed by Ldr Spine USA, United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Record published 2015-10-24
Record revised 2025-01-03 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Width 14 to 15.5 mm; depth 12 mm; height 5 to 9 mm

Catalogue Numbers

Catalogue numbers for ROI-C
Catalogue number Size Status
MC1354P Width 15.5 mm In distribution
MC1351P Width 15.5 mm In distribution
MC1345P Width 14 mm 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K162133 2017-05-16
K083857 2009-02-12
K080728 2008-05-29
K080569 2008-05-07
K080572 2008-04-07
K072132 2007-08-30
K043479 2005-06-30
K043349 2005-06-29

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