ARTiC-L™ 3d Ti Spinal System With TiONIC™ Technology

Spacer 56251510 12W 25MM X 15MM 10 DG TI

Registry build 21.09.26
14manufacturers in China registered for this device type
186catalogue 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 ARTiC-L™ 3D Ti Spinal System with TiONIC™ 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) K171689
Record published 2018-09-07
Record revised 2022-09-16 (version 9)

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
Sizes Angle 0 °; height 13 mm; length 25 mm

Catalogue Numbers

Catalogue numbers for ARTiC-L™ 3D Ti Spinal System with TiONIC™ Technology
Catalogue number Size Status
56251510 In distribution
56300805 In distribution
56301005 In distribution
5251005 In distribution
56301010 In distribution
56251410 In distribution
5251100 In distribution
56350810 In distribution
56301405 In distribution
56251205 In distribution
5251505 In distribution
56251005 In distribution
56351310 In distribution
56351505 In distribution
56351405 In distribution
56351205 In distribution
5251505 In distribution
56251210 In distribution
5251300 In distribution
5251220 In distribution
56351005 12W 35MM X 10MM 5 DG TI In distribution
56351505 In distribution
56251005 In distribution
56301010 In distribution
56350905 In distribution
56250805 In distribution
5250805 In distribution
5300800 In distribution
5251105 In distribution
5251120 In distribution
56301110 In distribution
5251320 In distribution
5251205 In distribution
5300805 In distribution
5330009 In distribution
56251505 In distribution
56251510 In distribution
5251220 In distribution
56251205 In distribution
5251500 In distribution
5251000 In distribution
56351320 In distribution
56301220 In distribution
56351420 In distribution
56251520 In distribution
56251010 In distribution
5251200 In distribution
56301520 In distribution
5251520 In distribution
5250900 In distribution
5251300 Angle 0.0 ° In distribution
56251120 In distribution
56351110 35mm x 11mm x 10DEG In distribution
56350810 In distribution
56350905 In distribution
56351110 In distribution
5251400 In distribution
56351105 In distribution
56251020 In distribution
5330009 In distribution
56301410 In distribution
56301320 In distribution
5250905 In distribution
56351310 In distribution
56251110 In distribution
56251310 In distribution
5251105 In distribution
56250910 In distribution
56301510 12W 30MM X 15MM 10 DG TI In distribution
5251120 In distribution
56301205 In distribution
56251105 In distribution
56350805 In distribution
56351520 In distribution
56301505 In distribution
5300805 In distribution
5250905 In distribution
56351220 In distribution
56250905 25mm x 9mm x 5DEG In distribution
56350805 In distribution
56251505 In distribution
56250805 In distribution
56251410 In distribution
56250810 In distribution
56300810 In distribution
56251210 In distribution
56351020 In distribution
56251010 In distribution
56301110 In distribution
56301520 In distribution
5350805 In distribution
56351320 In distribution
56301020 In distribution
56251105 In distribution
56251220 In distribution
5250800 In distribution
5251405 In distribution
56301210 12W 30MM X 12MM 10 DG TI In distribution
5332035 In distribution
56300910 In distribution
5350805 In distribution
56351410 In distribution
56250810 In distribution
56351020 In distribution
5250805 In distribution
56300905 In distribution
5251020 In distribution
56251405 In distribution
56301120 In distribution
56351210 12W 35MM X 12MM 10 DG TI In distribution
56251320 In distribution
56351510 In distribution
5332035 In distribution
56351420 In distribution
56301120 In distribution
56351120 In distribution
5251305 In distribution
56301220 In distribution
56301510 In distribution
56301005 In distribution
56251110 In distribution
56351010 In distribution
5330008 In distribution
56350910 In distribution
56251420 In distribution
56301310 In distribution
56301105 In distribution
56251420 In distribution
56351220 In distribution
56351510 In distribution
56350910 In distribution
56300810 In distribution
56251310 In distribution
56301305 In distribution
56301420 In distribution
5251420 In distribution
56251120 In distribution
56250910 In distribution
5251005 In distribution
56351205 In distribution
5251020 In distribution
56301210 In distribution
56251020 In distribution
56301105 In distribution
56351305 In distribution
56251520 In distribution
5251320 In distribution
56301405 In distribution
56251305 In distribution
5332033 In distribution
56251305 In distribution
5332034 In distribution
56301410 In distribution
56300910 In distribution
56301420 In distribution
56300805 In distribution
5251305 In distribution
56351005 In distribution
5332036 In distribution
56250905 In distribution
56351305 In distribution
5251205 In distribution
56351405 In distribution
56301020 In distribution
56351210 In distribution
5330008 In distribution
56301305 In distribution
56251405 In distribution
5251520 In distribution
5332034 In distribution
56251220 In distribution
56351120 In distribution
56251320 In distribution
56351520 In distribution
56300905 12W 30MM X 9MM 5 DG TI In distribution
56301310 30mm x 13mm x 10DEG In distribution
56351410 In distribution
5332033 In distribution
5350800 In distribution
56301205 In distribution
5251420 In distribution
56351010 12W 35MM X 10MM 10 DG TI In distribution
56351105 In distribution
56301505 In distribution
5251405 In distribution
56301320 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