Sustain

SUSTAIN Radiolucent Spacer, Medium, Narrow, Parallel, 9mm

Registry build 21.09.26
7manufacturers in China registered for this device type
48catalogue numbers in this listing
7510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code ODP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Sustain
Listed by Globus Medical, Inc., United States
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Manufacturer, Exporter
510(k) K040284
Record published 2015-11-06
Record revised 2025-07-14 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Label carries lot or batch number
Sizes Width 12 to 14 mm; height 5 to 12 mm; depth 11 to 13 mm

Catalogue Numbers

Catalogue numbers for Sustain
Catalogue number Size Status
304.249 Width 14 mm In distribution
101.248 Height 8 mm In distribution
304.066 Width 14 mm In distribution
304.909 Width 12 mm In distribution
101.249 Height 9 mm In distribution
304.232 Depth 13 mm In distribution
101.831 Depth 11 mm In distribution
101.845 Width 12 mm In distribution
304.206 Depth 13 mm In distribution
304.270 Depth 13 mm In distribution
101.805 Width 12 mm In distribution
304.210 Width 14 mm In distribution
101.827 Depth 11 mm In distribution
101.809 Width 12 mm In distribution
101.810 Depth 11 mm In distribution
304.072 Depth 13 mm In distribution
101.209 Height 9 mm In distribution
101.230 Depth 13 mm In distribution
304.231 Lordosis 7 Degree In distribution
304.067 Width 14 mm In distribution
101.207 Width 14 mm In distribution
101.232 Width 14 mm In distribution
304.229 Depth 13 mm In distribution
101.212 Depth 13 mm In distribution
304.228 Height 8 mm In distribution
304.277 Height 7 mm In distribution
101.206 Depth 13 mm In distribution
101.812 Width 12 mm In distribution
304.905 Depth 11 mm In distribution
101.850 Width 12 mm In distribution
101.252 Width 14 mm In distribution
304.230 Height 10 mm In distribution
304.950 Depth 11 mm In distribution
304.947 Height 7 mm In distribution
304.925 Lordosis 7 Degree In distribution
101.229 Lordosis 7 Degree In distribution
101.210 Height 10 mm In distribution
101.852 Width 12 mm In distribution
304.952 Height 12 mm In distribution
304.906 Height 6 mm In distribution
304.280 Lordosis 7 Degree In distribution
101.227 Height 7 mm In distribution
304.276 Lordosis 7 Degree In distribution
101.811 Width 12 mm In distribution
101.246 Height 6 mm In distribution
304.282 Lordosis 7 Degree In distribution
101.806 Width 12 mm In distribution
101.832 Lordosis 7 Degree In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K222270 2022-10-21
K191243 2019-09-17
K180909 2018-12-18
K173722 2018-05-23
K173115 2017-12-20
K142218 2015-03-31
K072991 2008-01-18

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