Cambria™

Cambria Implant, 17mm x 13mm x 12mm, Lordotic

Registry build 21.09.26
3manufacturers in China registered for this device type
36catalogue 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 Cambria™
Listed by Seaspine Orthopedics Corporation, United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K052170
Record published 2016-11-09
Record revised 2025-10-24 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2016-09-02

Catalogue Numbers

Catalogue numbers for Cambria™
Catalogue number Size Status
39-1707 17mm x 13mm x 7mm In distribution
39-1711 17mm x 13mm x 11mm In distribution
39-1708 17mm x 13mm x 8mm In distribution
39-1710 17mm x 13mm x 10mm In distribution
39-1709 17mm x 13mm x 9mm In distribution
39-1706 17mm x 13mm x 6mm In distribution
39-1712 17mm x 13mm x 12mm In distribution
39-1705 17mm x 13mm x 5mm In distribution
93-9111 13mm x 12mm x 11mm In distribution
93-9110 13mm x 12mm x 10mm In distribution
39-1712 17mm x 13mm x 12mm Withdrawn
93-9125 13mm x 12mm x 5mm Withdrawn
39-1707 17mm x 13mm x 7mm Withdrawn
39-1711 17mm x 13mm x 11mm Withdrawn
39-1709 17mm x 13mm x 9mm Withdrawn
93-9138 13mm x 12mm x 8mm Withdrawn
93-9140 13mm x 12mm x 10mm Withdrawn
93-9142 13mm x 12mm x 12mm Withdrawn
93-9136 13mm x 12mm x 6mm Withdrawn
93-9129 13mm x 12mm x 9mm Withdrawn
93-9126 13mm x 12mm x 6mm Withdrawn
93-9131 13mm x 12mm x 11mm Withdrawn
93-9135 13mm x 12mm x 5mm Withdrawn
39-1706 17mm x 13mm x 6mm Withdrawn
93-9127 13mm x 12mm x 7mm Withdrawn
93-9128 13mm x 12mm x 8mm Withdrawn
93-9111 13mm x 12mm x 11mm Withdrawn
93-9141 13mm x 12mm x 11mm Withdrawn
39-1708 17mm x 13mm x 8mm Withdrawn
93-9139 13mm x 12mm x 9mm Withdrawn
93-9137 13mm x 12mm x 7mm Withdrawn
39-1705 17mm x 13mm x 5mm Withdrawn
93-9110 13mm x 12mm x 10mm Withdrawn
39-1710 17mm x 13mm x 10mm Withdrawn
93-9130 13mm x 12mm x 10mm Withdrawn
93-9132 13mm x 12mm x 12mm Withdrawn

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

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