Evol Lumbar Interbody System

15X17mm,X 10mm X 23 mm HA PEEK, Lordotic LIF Cage

Registry build 21.09.26
14manufacturers in China registered for this device type
114catalogue numbers in this listing
6510(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 Evol Lumbar Interbody System
Listed by Cutting Edge Spine, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K102957
Record published 2015-10-30
Record revised 2024-09-11 (version 7)

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
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store at room temperature
Sizes Length 23 to 55 mm; length 14 in
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Evol Lumbar Interbody System
Catalogue number Size Status
CLB16012 Length 50 mm In distribution
CLB36013 Length 55 mm In distribution
CLB16016 Length 50 mm In distribution
CLB26009 Length 45 mm In distribution
CLB16007 Length 50 mm In distribution
CPB03014 Length 27 mm In distribution
CLB26008 Length 45 mm In distribution
CPB01011 Length 23 mm In distribution
CPB01010 Length 23 mm In distribution
CLB11017 Length 23 mm In distribution
CLB03011 Length 27 mm In distribution
CLB11009 Length 23 mm In distribution
CLB03012 Length 27 mm In distribution
CLB16015 Length 50 mm In distribution
CPB15011 Length 32 mm In distribution
CLB16008 Length 50 mm In distribution
CLB36012 Length 55 mm In distribution
CPB05013 Length 28 mm In distribution
HLB04010 Length 23 mm In distribution
CLB03008 Length 27 mm In distribution
CLB36017 Length 55 mm In distribution
CLB06016 Length 40 mm In distribution
CLB06013 Length 40 mm In distribution
CLB04017 Length 23 mm In distribution
CES-127 Length 14 in In distribution
CLB16014 Length 50 mm In distribution
CPB01014 Length 23 mm In distribution
CLB16011 Length 50 mm In distribution
CPB01016 Length 23 mm In distribution
CLB26011 Length 45 mm In distribution
CLB26013 Length 45 mm In distribution
CLB06015 Length 40 mm In distribution
CLB06012 Length 40 mm In distribution
CLB04013 Length 23 mm In distribution
CLB36015 Length 55 mm In distribution
CLB04011 Length 23 mm In distribution
CLB36009 Length 55 mm In distribution
CPB03015 Length 27 mm In distribution
CPB03011 Length 27 mm In distribution
HLB04017 Length 23 mm In distribution
CLB03015 Length 27 mm In distribution
HLB04015 Length 23 mm In distribution
CPB01007 Length 23 mm In distribution
CPB05012 Length 28 mm In distribution
CLB11011 Length 23 mm In distribution
CPB03012 Length 27 mm In distribution
CLB16013 Length 50 mm In distribution
CLB03009 Length 27 mm In distribution
CLB03010 Length 27 mm In distribution
CLB36007 Length 55 mm In distribution
CPB05016 Length 28 mm In distribution
CLB11012 Length 23 mm In distribution
CPB05008 Length 28 mm In distribution
CLB36010 Length 55 mm In distribution
CLB26017 Length 45 mm In distribution
CLB26012 Length 45 mm In distribution
CPB15008 Length 32 mm In distribution
CLB26007 Length 45 mm In distribution
CPB15010 Length 32 mm In distribution
CLB11013 Length 23 mm In distribution
CLB11010 Length 23 mm In distribution
CLB06011 Length 40 mm In distribution
CLB36016 Length 55 mm In distribution
CLB16009 Length 50 mm In distribution
CLB04009 Length 50 mm In distribution
CPB03010 Length 27 mm In distribution
CPB01008 Length 23 mm In distribution
CLB03013 Length 27 mm In distribution
CPB15013 Length 32 mm In distribution
HLB04013 Length 23 mm In distribution
CPB01009 Length 23 mm In distribution
CLB06009 Length 40 mm In distribution
CLB26014 Length 45 mm In distribution
CPB05015 Length 28 mm In distribution
CPB15012 Length 32 mm In distribution
CPB03013 Length 27 mm In distribution
CPB01012 Length 23 mm In distribution
CPB05009 Length 28 mm In distribution
HLB04016 Length 23 mm In distribution
HLB04014 Length 23 mm In distribution
CLB16010 Length 50 mm In distribution
CLB36014 Length 55 mm In distribution
CLB11015 Length 23 mm In distribution
CPB05014 Length 28 mm In distribution
CLB11016 Length 23 mm In distribution
CLB06008 Length 40 mm In distribution
CPB03008 Length 27 mm In distribution
CLB26016 Length 45 mm In distribution
CPB15014 Length 32 mm In distribution
CPB05011 Length 28 mm In distribution
CPB01015 Length 23 mm In distribution
CLB03014 Length 27 mm In distribution
CLB06014 Length 40 mm In distribution
HLB04011 Length 23 mm In distribution
CLB06010 Length 40 mm In distribution
CLB16017 Length 50 mm In distribution
CPB15009 Length 32 mm In distribution
CLB06007 Length 40 mm In distribution
CPB15015 Length 32 mm In distribution
CLB04015 Length 23 mm In distribution
CLB36008 Length 55 mm In distribution
HLB04012 Length 23 mm In distribution
CPB01013 Length 23 mm In distribution
HLB04009 Length 23 mm In distribution
CES-241 Length 14 in In distribution
CLB26010 Length 45 mm In distribution
CPB01017 Length 23 mm In distribution
CPB05010 Length 28 mm In distribution
CPB15016 Length 32 mm In distribution
CPB03009 Length 27 mm In distribution
CLB11014 Length 23 mm In distribution
CLB06017 Length 40 mm In distribution
CLB26015 Length 45 mm In distribution
CLB36011 Length 55 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
K200991 2020-05-13
K200552 2020-04-02
K192497 2020-01-06
K180891 2018-05-04
K150321 2015-07-13
K102957 2011-04-28

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