Solitaire-C Cervical Spacer SYS

32 catalogue numbers from 14-531726, listed by Biomet Spine, United States, under Intervertebral Fusion Device With Integrated Fixation, Cervical. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
32catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (1), Jiangsu (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVE
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for Solitaire-C Cervical Spacer SYS
Listed by Biomet Spine, United States
FDA product code OVE
Device type Intervertebral Fusion Device With Integrated Fixation, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Record published 2015-10-24
Record revised 2025-07-02 (version 6)

Specifications

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

Catalogue Numbers

Catalogue numbers for Solitaire-C Cervical Spacer SYS
Catalogue number Size Status
14-531726 SOLI-C 3.75X16MM SCREW In distribution
14-531722E SOLI-C 3.75MM X 12MM SCREW In distribution
14-531728E SOLI-C 3.75MM X 18MM SCREW In distribution
14-531713 SOLI-C 3.5X13MM SCREW In distribution
14-531713E SOLI-C 3.5MM X 13MM SCREW In distribution
14-531715E SOLI-C 3.5MM X 15MM SCREW In distribution
14-531715 SOLI-C 3.5X15MM SCREW In distribution
14-531718 SOLI-C 3.5X18MM SCREW In distribution
14-531726E SOLI-C 3.75MM X 16MM SCREW In distribution
14-531722 SOLI-C 3.75X12MM SCREW In distribution
14-531725 SOLI-C 3.75X15MM SCREW In distribution
14-531718E SOLI-C 3.5MM X 18MM SCREW In distribution
14-531723 SOLI-C 3.75X13MM SCREW In distribution
14-531725E SOLI-C 3.75MM X 15MM SCREW In distribution
14-531728 SOLI-C 3.75X18MM SCREW In distribution
14-531727E SOLI-C 3.75MM X 17MM SCREW In distribution
14-531721E SOLI-C 3.75MM X 11MM SCREW In distribution
14-531717E SOLI-C 3.5MM X 17MM SCREW In distribution
14-531711E SOLI-C 3.5MM X 11MM SCREW In distribution
14-531724 SOLI-C 3.75X14MM SCREW In distribution
14-531724E SOLI-C 3.75MM X 14MM SCREW In distribution
14-531714E SOLI-C 3.5MM X 14MM SCREW In distribution
14-531716 SOLI-C 3.5X16MM SCREW In distribution
14-531716E SOLI-C 3.5MM X 16MM SCREW In distribution
14-531723E SOLI-C 3.75MM X 13MM SCREW In distribution
14-531711 SOLI-C 3.5X11MM SCREW In distribution
14-531712E SOLI-C 3.5MM X 12MM SCREW In distribution
14-531714 SOLI-C 3.5X14MM SCREW In distribution
14-531721 SOLI-C 3.75X11MM SCREW In distribution
14-531727 SOLI-C 3.75X17MM SCREW In distribution
14-531712 SOLI-C 3.5X12MM SCREW In distribution
14-531717 SOLI-C 3.5X17MM SCREW In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
IdentiTi Alphatec Spine, Inc. 630
Dolomite Astura Medical 607
CoRoent Nuvasive, Inc. 580
Aeon-C Diomedical Co., Ltd. 508
Tomcat™ Cervical Spinal System Choice Spine, LP 468
Shoreline ACS Seaspine Orthopedics Corporation 428
Zavation Zavation 423
Alta™ Stand-Alone Interbody Fusion System Biomet Spine 404
Unison™-C Anterior Cervical Fixation System Pioneer Surgical Technology, Inc. 334
Chesapeake® Stabilization System VB Spine LLC 272
UniSpace® Stand-Alone C Cage CG MedTech Co., Ltd. 260
Solitaire-C Cervical Spacer Biomet Spine 256

Showing 12 of 391. All products under Intervertebral Fusion Device With Integrated Fixation, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K152622 2016-07-08
K151064 2015-08-12

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