Elevate™ Spinal System

Instr Innr Locking Tube 8657002 Elevate

Registry build 21.09.26
14manufacturers in China registered for this device type
37catalogue 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 Elevate™ 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) K142559
Record published 2015-09-30
Record revised 2024-09-11 (version 7)

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 Height 7 to 32 mm; length 10 to 32 mm; width 10 mm

Catalogue Numbers

Catalogue numbers for Elevate™ Spinal System
Catalogue number Size Status
7771028 Length 28.0 mm In distribution
8657001 In distribution
8880923 Width 10.0 mm In distribution
8657005 In distribution
8657003 In distribution
8881132 Height 32.0 mm In distribution
8657003 In distribution
7770723 Width 10.0 mm In distribution
8881123 Height 11.0 mm In distribution
8657002 In distribution
8657001 In distribution
7770928 Length 28.0 mm In distribution
8880828 Height 8.0 mm In distribution
8880823 Height 8.0 mm In distribution
7770732 Length 32.0 mm In distribution
8881032 Length 32.0 mm In distribution
7771123 Height 11.0 mm In distribution
7770728 Height 7.0 mm In distribution
8657002 In distribution
8657006 In distribution
7770923 Length 23.0 mm In distribution
8881028 Width 10.0 mm In distribution
8881128 Width 10.0 mm In distribution
8657008 In distribution
8880832 Length 32.0 mm In distribution
7771132 Length 32.0 mm In distribution
8880932 Height 9.0 mm In distribution
7770832 Width 10.0 mm In distribution
8657007 In distribution
7771128 Length 28.0 mm In distribution
7770932 Height 9.0 mm In distribution
8880928 Width 10.0 mm In distribution
7771023 Width 10.0 mm In distribution
7771032 Length 32.0 mm In distribution
7770823 Height 8.0 mm In distribution
7770828 Width 10.0 mm In distribution
8881023 Width 10.0 mm 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