XLX

XLX ACR Cutter, Ant LongitudLigament Nrw

Registry build 21.09.26
3manufacturers in China registered for this device type
34catalogue numbers in this listing
4510(k) clearances naming this product code

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 XLX
Listed by Nuvasive, Inc., United States
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K173892
Record published 2018-07-02
Record revised 2025-06-11 (version 8)

Specifications

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

Catalogue Numbers

Catalogue numbers for XLX
Catalogue number Size Status
1676704 In distribution
1675082 In distribution
1676708 In distribution
1676699 In distribution
1675080 In distribution
1676670 In distribution
1676912 In distribution
1676693 In distribution
1676940 In distribution
1845203 In distribution
1676634 In distribution
1676916 In distribution
1676918 In distribution
1675075 In distribution
1676919 In distribution
1677001 In distribution
1676701 In distribution
1676707 In distribution
D1676640 In distribution
1871540 In distribution
1676911 In distribution
1675076 In distribution
1676914 In distribution
1871560 In distribution
1871521 In distribution
1675079 In distribution
1676910 In distribution
1676631 In distribution
1871530 In distribution
1676702 In distribution
1871520 In distribution
1675085 In distribution
D1676601 In distribution
1676709 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
K131723 2013-09-20
K123045 2013-04-16
K112561 2012-03-13
K100043 2010-06-16

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