Capstone Control™ Spinal System

Spacer X1217025 10X18MM 12 DEG CAP Cntrl

Registry build 21.09.26
14manufacturers in China registered for this device type
111catalogue 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 Capstone Control™ Spinal System
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) K120368
Record published 2015-06-25
Record revised 2025-11-18 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Sizes Length 18 to 32 mm; angle 0 to 24 °; outer diameter 8 to 17 mm; height 8 to 18 mm
Distribution end date 2025-11-11

Catalogue Numbers

Catalogue numbers for Capstone Control™ Spinal System
Catalogue number Size Status
3991732 Length 32.0 mm In distribution
X1217024 Height 9.0 mm In distribution
3991632 Angle 0.0 ° In distribution
3991132 Angle 0.0 ° In distribution
4001227 Length 27.0 mm In distribution
4001722 Angle 6.0 ° In distribution
4031522 Angle 24.0 ° In distribution
X1217025 Height 10.0 mm In distribution
3991422 Angle 0.0 ° In distribution
4021427 Outer Diameter 14.0 mm In distribution
4001522 Angle 6.0 ° In distribution
4021727 Outer Diameter 17.0 mm In distribution
4001132 Length 32.0 mm In distribution
4011422 Outer Diameter 14.0 mm In distribution
4011322 Angle 12.0 ° In distribution
4001632 Angle 6.0 ° In distribution
X1217034 Length 18.0 mm In distribution
4001627 Outer Diameter 16.0 mm In distribution
X1217028 Height 10.0 mm In distribution
3991727 Outer Diameter 17.0 mm In distribution
3991722 Angle 0.0 ° In distribution
4021627 Length 27.0 mm In distribution
X1217020 Height 8.0 mm In distribution
X1217017 Length 18.0 mm In distribution
3991627 Length 27.0 mm In distribution
X1217033 Length 18.0 mm In distribution
4001732 Outer Diameter 17.0 mm In distribution
X1217030 Angle 6.0 ° In distribution
3991622 Length 22.0 mm In distribution
X1217018 Height 9.0 mm In distribution
4001727 Angle 6.0 ° In distribution
3991527 Angle 0.0 ° In distribution
3991227 Angle 0.0 ° In distribution
4001422 Angle 6.0 ° In distribution
4021622 Outer Diameter 16.0 mm In distribution
3991332 Angle 0.0 ° In distribution
3990927 Outer Diameter 9.0 mm In distribution
X1217031 Length 18.0 mm In distribution
X1217021 Height 9.0 mm In distribution
4001322 Length 22.0 mm In distribution
4001127 Length 22.0 mm In distribution
3991222 Angle 0.0 ° In distribution
3990827 Angle 0.0 ° In distribution
4021322 Angle 18.0 ° In distribution
4001527 Angle 6.0 ° In distribution
X1217029 Height 8.0 mm In distribution
3991532 Angle 0.0 ° In distribution
4011222 Angle 12.0 ° In distribution
4001532 Outer Diameter 15.0 mm In distribution
4021522 Outer Diameter 12.0 mm In distribution
4011622 Outer Diameter 16.0 mm In distribution
4011427 Angle 12.0 ° In distribution
4021422 Outer Diameter 14.0 mm In distribution
3990822 Length 22.0 mm In distribution
4011627 Length 27.0 mm In distribution
4011727 Angle 12.0 ° In distribution
4031527 Length 27.0 mm In distribution
4001122 Length 22.0 mm In distribution
X1217023 Angle 12.0 ° In distribution
3990922 Outer Diameter 9.0 mm In distribution
X1217027 Length 18.0 mm In distribution
4031422 Height 14.0 mm In distribution
4011122 Outer Diameter 11.0 mm In distribution
3991032 Angle 0.0 ° In distribution
4001232 Length 32.0 mm In distribution
3991232 Outer Diameter 12.0 mm In distribution
4001432 Outer Diameter 14.0 mm In distribution
X1217022 Length 18.0 mm In distribution
3991127 Angle 0.0 ° In distribution
3991522 Angle 0.0 ° In distribution
4001427 Angle 6.0 ° In distribution
4011527 Length 27.0 mm In distribution
4011722 Angle 12.0 ° In distribution
3991427 Angle 0.0 ° In distribution
4001622 Length 22.0 mm In distribution
4001027 Length 27.0 mm In distribution
4001022 Length 22.0 mm In distribution
3991122 Angle 0.0 ° In distribution
4011227 Outer Diameter 12.0 mm In distribution
4021722 Length 22.0 mm In distribution
3991022 Outer Diameter 10.0 mm In distribution
4021527 Outer Diameter 15.0 mm In distribution
3991327 Angle 0.0 ° In distribution
4011522 Angle 12.0 ° In distribution
4011327 Length 27.0 mm In distribution
4001332 Length 32.0 mm In distribution
4011022 Length 22.0 mm In distribution
4001327 Angle 6.0 ° In distribution
X1217032 Angle 12.0 ° In distribution
3991027 Angle 0.0 ° In distribution
3991322 Outer Diameter 13.0 mm In distribution
4001222 Outer Diameter 12.0 mm In distribution
4031322 Height 13.0 mm In distribution
X1217019 Height 10.0 mm In distribution
X1217026 Height 8.0 mm In distribution
3991432 Angle 0.0 ° In distribution
4031822 Length 22.0 mm Withdrawn
X1012418 Angle 0.0 ° Withdrawn
X1012416 Angle 0.0 ° Withdrawn
X1012413 Height 11.0 mm Withdrawn
X1012411 Length 22.0 mm Withdrawn
X1012415 Height 13.0 mm Withdrawn
X1012420 Angle 0.0 ° Withdrawn
X1012421 Angle 0.0 ° Withdrawn
X1012410 Angle 0.0 ° Withdrawn
X1012419 Height 17.0 mm Withdrawn
X1012412 Angle 0.0 ° Withdrawn
4031622 Height 16.0 mm Withdrawn
4031722 Angle 24.0 ° Withdrawn
X1012417 Angle 0.0 ° Withdrawn
X1012414 Length 22.0 mm Withdrawn

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