Colorado 2™ Spinal System

Connector 8635400 5.5X5.5 LAT Close Clmp

Registry build 21.09.26
13manufacturers in China registered for this device type
43catalogue numbers in this listing
23510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNI
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Changzhou Yonghua Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 8
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7

Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spinal Pedicle Fixation

Record

Regulatory record for Colorado 2™ Spinal System
Listed by Medtronic Sofamor Danek, Inc., United States
FDA product code MNI
Device type Orthosis, Spinal Pedicle Fixation
Device class Class 2
Regulation 21 CFR 888.3070
510(k) K991031
Record published 2015-08-04
Record revised 2025-12-23 (version 7)

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
Sizes Length 30 to 340 mm; outer diameter 4.5 to 7.5 mm
Distribution end date 2025-12-22

Catalogue Numbers

Catalogue numbers for Colorado 2™ Spinal System
Catalogue number Size Status
8632255 Length 55.0 mm In distribution
8635400 In distribution
8612240 Length 40.0 mm In distribution
8638750 Length 50.0 mm In distribution
8612245 Length 45.0 mm In distribution
8638440 Outer Diameter 4.5 mm In distribution
8638120 In distribution
8638535 Length 35.0 mm In distribution
8632230 Length 30.0 mm In distribution
XA600909 In distribution
8614111 In distribution
8612235 Length 35.0 mm In distribution
X8632050 Outer Diameter 7.0 mm In distribution
8632265 Length 65.0 mm In distribution
8638203 In distribution
8638650 Length 50.0 mm In distribution
8612060 Length 60.0 mm In distribution
8611203 In distribution
8613518 Length 180.0 mm In distribution
8613508 Length 80.0 mm In distribution
8638635 Outer Diameter 6.5 mm In distribution
8631402 In distribution
8638110 In distribution
X09204040 Length 40.0 mm Withdrawn
8612365 Length 65.0 mm Withdrawn
8632050 Length 50.0 mm Withdrawn
8613534 Length 340.0 mm Withdrawn
8612370 Length 70.0 mm Withdrawn
8613511 Length 110.0 mm Withdrawn
8619110 Withdrawn
8631202 Withdrawn
8639400 Withdrawn
8610645 Length 45.0 mm Withdrawn
8612335 Length 35.0 mm Withdrawn
8610635 Length 35.0 mm Withdrawn
8615400 5.0 mm/5.0 mm Withdrawn
8610430 Length 30.0 mm Withdrawn
8611202 Withdrawn
8613528 Length 280.0 mm Withdrawn
8611102 Withdrawn
8610665 Length 65.0 mm Withdrawn
8613532 Length 320.0 mm Withdrawn
8611402 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,342
Creo Globus Medical, Inc. 1,784
ReLine Nuvasive, Inc. 1,718
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 1,525
Apex Spine System Spinecraft LLC 1,114
Revere Globus Medical, Inc. 1,051
LnK Spinal Fixation System L&K Biomed Co., Ltd. 974
LnK Basic Spinal Fixation System L&K Biomed Co., Ltd. 935
Arsenal Alphatec Spine, Inc. 932
Zavation Zavation 864
Polaris™ 5.5 Spinal System Biomet Spine 809
Apex-DL Spine System Spinecraft LLC 792

Showing 12 of 950. All products under Orthosis, Spinal Pedicle Fixation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K062879 2006-12-22
K062606 2006-09-25
K053483 2006-01-05
K042210 2004-11-04
K042453 2004-10-07
K041777 2004-09-03
K041030 2004-06-30
K041118 2004-05-28
K040583 2004-03-31
K033495 2003-12-03
K033271 2003-11-06
K031967 2003-09-17
K032578 2003-09-17
K032037 2003-09-04
K031833 2003-09-03
K031888 2003-06-27
K030932 2003-05-16
K030840 2003-05-15
K022778 2002-09-18
K021106 2002-05-03
K011029 2001-06-05
K011067 2001-05-04
K000991 2000-04-18

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Colorado 2™ Spinal System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Warsaw Orthopedic, Inc. 510(k) number 2007-09-10 Not classified Process control Assembly may be compromised: Two thread grooves are missing on the nut, which may cause damage to the bone screw and result in the need for the bone screw to be replaced. 2,569 2009-07-14

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