Anteralign Spinal System With Titan Nanolock Surface Technology

Nano Spacer 46321450 TI 12DG 23W 14X50MM

Registry build 21.09.26
14manufacturers in China registered for this device type
95catalogue numbers in this listing
18510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for Anteralign Spinal System with Titan nanoLock Surface technology
Listed by Medtronic Sofamor Danek, Inc., United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K212524
Record published 2022-02-21
Record revised 2025-07-14 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Anteralign Spinal System with Titan nanoLock Surface technology
Catalogue number Size Status
46361045 In distribution
46321450 In distribution
46501214 In distribution
46521218 In distribution
46813614 In distribution
4675025 In distribution
46321245 In distribution
46821220 In distribution
46812816 In distribution
46261060 In distribution
46510614 In distribution
46501218 In distribution
46500610 In distribution
46321050 In distribution
46261260 In distribution
46841223 In distribution
46501216 In distribution
46812210 In distribution
46261050 In distribution
46820418 In distribution
46512418 In distribution
46361450 In distribution
46360845 In distribution
4675040 In distribution
46812616 In distribution
4680004 In distribution
46813608 In distribution
46261240 In distribution
46341460 In distribution
46813610 In distribution
46841220 In distribution
46381455 In distribution
46813820 In distribution
46822816 In distribution
46813212 In distribution
46813418 In distribution
46820416 In distribution
46502416 In distribution
46513020 In distribution
46341660 In distribution
46511816 In distribution
46361055 In distribution
46321055 In distribution
46511210 In distribution
46261055 In distribution
46381845 In distribution
46321445 In distribution
46321045 In distribution
46500614 In distribution
46812608 In distribution
4680005 In distribution
46341650 In distribution
46812420 In distribution
46812814 In distribution
46501210 In distribution
4675150 In distribution
46261445 In distribution
46321240 In distribution
46813210 In distribution
46260855 In distribution
46501816 In distribution
46341655 In distribution
46221045 In distribution
4675125 In distribution
46813814 In distribution
46812414 In distribution
46321455 In distribution
46820812 In distribution
46321460 In distribution
46812612 In distribution
46501814 In distribution
46520614 In distribution
46822418 In distribution
46503018 In distribution
46812212 In distribution
46261045 In distribution
46521214 In distribution
46521818 In distribution
46360850 In distribution
46511216 In distribution
46831223 In distribution
46361455 In distribution
46361245 In distribution
46812216 In distribution
46822616 In distribution
46361050 In distribution
46361250 In distribution
46221060 In distribution
46820318 In distribution
NAV4680003 In distribution
46501818 In distribution
46812214 In distribution
46813218 In distribution
46221050 In distribution
46521216 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201267 2020-08-26
K172199 2017-09-19
K171031 2017-07-06
K171468 2017-06-13
K132897 2013-12-11
K133216 2013-11-22
K132700 2013-09-26
K123027 2013-07-25
K122037 2013-03-22
K122591 2012-09-18
K111525 2011-08-24
K103731 2011-07-18
K100175 2010-06-02
K094025 2010-04-26
K090353 2009-09-29
K083026 2008-12-29
K082342 2008-09-12
K080083 2008-04-10

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

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