Gladstone Alif Trial Cage

63 catalogue numbers from W32-04-0242, listed by Signature Orthopaedics PTY Limited, Australia, under Intervertebral Fusion Device With Integrated Fixation, Lumbar. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
63catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

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

Chinese manufacturers registered for FDA product code OVD
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
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Gladstone Alif Trial Cage
Listed by Signature Orthopaedics PTY Limited, Australia
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K172019
Record published 2018-10-05
Record revised 2020-07-02 (version 3)

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

Catalogue Numbers

Catalogue numbers for Gladstone Alif Trial Cage
Catalogue number Size Status
W32-04-0242 In distribution
W32-04-0212 In distribution
W32-04-0240 In distribution
W32-04-0256 In distribution
W32-04-0226 In distribution
W32-04-0254 In distribution
W32-04-0238 In distribution
W32-04-0241 In distribution
W32-04-0258 In distribution
W32-04-0206 In distribution
W32-04-0215 In distribution
W32-04-0230 In distribution
W32-04-0236 In distribution
W32-04-0252 In distribution
W32-04-0250 In distribution
W32-04-0259 In distribution
W32-04-0211 In distribution
W32-04-0214 In distribution
W32-04-0233 In distribution
W32-04-0247 In distribution
W32-04-0208 In distribution
W32-04-0263 In distribution
W32-04-0224 In distribution
W32-04-0228 In distribution
W32-04-0227 In distribution
W32-04-0251 In distribution
W32-04-0253 In distribution
W32-04-0218 In distribution
W32-04-0245 In distribution
W32-04-0213 In distribution
W32-04-0210 In distribution
W32-04-0225 In distribution
W32-04-0248 In distribution
W32-04-0203 In distribution
W32-04-0249 In distribution
W32-04-0260 In distribution
W32-04-0221 In distribution
W32-04-0207 In distribution
W32-04-0257 In distribution
W32-04-0235 In distribution
W32-04-0234 In distribution
W32-04-0261 In distribution
W32-04-0204 In distribution
W32-04-0222 In distribution
W32-04-0209 In distribution
W32-04-0216 In distribution
W32-04-0246 In distribution
W32-04-0217 In distribution
W32-04-0237 In distribution
W32-04-0219 In distribution
W32-04-0220 In distribution
W32-04-0232 In distribution
W32-04-0231 In distribution
W32-04-0243 In distribution
W32-04-0262 In distribution
W32-04-0201 In distribution
W32-04-0200 In distribution
W32-04-0202 In distribution
W32-04-0244 In distribution
W32-04-0255 In distribution
W32-04-0229 In distribution
W32-04-0223 In distribution
W32-04-0239 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sirion Astura Medical 1,465
IdentiTi Alphatec Spine, Inc. 1,372
EL Capitan Astura Medical 1,205
Zavation Zavation 1,157
Brigade Nuvasive, Inc. 1,005
Solar™ Interbody Fusion System Degen Medical 899
Zavation F3D Corpectomy Zavation 730
ROI-A Ldr Spine USA 552
Avenue L Ldr Spine USA 524
Transcend Nanotec Alphatec Spine, Inc. 485
Endoskeleton® TL Hyperlordotic nanoLOCK® Surface Technology Titan Spine, LLC 462
Base Nuvasive, Inc. 462

Showing 12 of 241. All products under Intervertebral Fusion Device With Integrated Fixation, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K172019 2017-11-29

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