Cezanne II Lumbar Interbody Fusion Cage System

CEZANNE-II™ DLIF PEEK Cage, 12Deg., W19 x L40, H16mm

Registry build 21.09.26
14manufacturers in China registered for this device type
312catalogue numbers in this listing
4510(k) clearances naming this product code
4recalls on this 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 Cezanne II Lumbar Interbody Fusion Cage System
Listed by CTL Medical Corporation, 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, Complaint-file establishment, Manufacturer
510(k) K131981
Record published 2024-01-07
Record revised 2026-03-17 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for Cezanne II Lumbar Interbody Fusion Cage System
Catalogue number Size Status
018.3010 In distribution
018.4512 In distribution
018.2615 In distribution
018.4309 In distribution
018.4515 In distribution
018.3212 In distribution
018.4516 In distribution
018.4215 In distribution
018.3014 In distribution
018.1310 In distribution
018.3516 In distribution
018.2909 In distribution
018.4811 In distribution
018.3810 In distribution
018.4612 In distribution
018.2813 In distribution
018.2916 In distribution
018.4212 In distribution
018.3115 In distribution
018.4308 In distribution
018.4616 In distribution
018.3108 In distribution
018.4416 In distribution
018.4710 In distribution
018.3916 In distribution
018.3713 In distribution
018.2616 In distribution
018.3011 In distribution
018.5013 In distribution
018.4108 In distribution
018.3912 In distribution
018.4313 In distribution
018.4412 In distribution
018.1708 In distribution
018.5209 In distribution
018.3808 In distribution
018.3113 In distribution
018.2815 In distribution
018.3412 In distribution
018.2511 In distribution
018.3714 In distribution
018.4909 In distribution
018.3114 In distribution
018.3514 In distribution
018.4814 In distribution
018.5008 In distribution
018.3214 In distribution
018.1115 In distribution
018.1315 In distribution
018.3908 In distribution
018.1913 In distribution
018.2910 In distribution
018.5414 In distribution
018.4608 In distribution
018.1116 In distribution
018.3814 In distribution
018.4015 In distribution
018.5216 In distribution
018.3813 In distribution
018.3715 In distribution
018.2714 In distribution
018.4816 In distribution
018.2812 In distribution
018.3513 In distribution
018.5416 In distribution
018.4715 In distribution
018.3811 In distribution
018.4613 In distribution
018.1712 In distribution
018.4009 In distribution
018.5309 In distribution
018.4815 In distribution
018.4214 In distribution
018.5010 In distribution
018.5210 In distribution
018.4216 In distribution
018.4208 In distribution
018.5116 In distribution
018.3016 In distribution
018.5215 In distribution
018.2712 In distribution
018.3609 In distribution
018.2609 In distribution
018.4415 In distribution
018.2512 In distribution
018.1709 In distribution
018.4916 In distribution
018.3109 In distribution
018.1114 In distribution
018.2716 In distribution
018.1108 In distribution
018.2711 In distribution
018.1915 In distribution
018.4110 In distribution
018.1713 In distribution
018.5113 In distribution
018.4914 In distribution
018.3612 In distribution
018.3512 In distribution
018.3608 In distribution
018.5111 In distribution
018.4111 In distribution
018.4609 In distribution
018.1908 In distribution
018.4210 In distribution
018.5415 In distribution
018.3309 In distribution
018.1911 In distribution
018.7700 In distribution
018.5115 In distribution
018.4312 In distribution
018.2608 In distribution
018.3416 In distribution
018.3712 In distribution
018.3816 In distribution
018.4915 In distribution
018.4809 In distribution
018.3312 In distribution
018.5009 In distribution
018.1113 In distribution
018.5212 In distribution
018.4709 In distribution
018.3116 In distribution
018.3415 In distribution
018.3310 In distribution
018.3410 In distribution
018.3216 In distribution
018.3211 In distribution
018.2810 In distribution
018.4114 In distribution
018.4113 In distribution
018.4213 In distribution
018.2913 In distribution
018.5315 In distribution
018.1710 In distribution
018.5409 In distribution
018.4314 In distribution
018.2610 In distribution
018.3710 In distribution
018.2713 In distribution
018.8400 In distribution
018.4712 In distribution
018.2614 In distribution
018.3613 In distribution
018.2510 In distribution
018.4013 In distribution
018.5313 In distribution
018.4912 In distribution
018.3110 In distribution
018.1109 In distribution
018.3013 In distribution
018.1309 In distribution
018.4812 In distribution
018.3911 In distribution
018.4508 In distribution
018.2915 In distribution
018.4913 In distribution
018.4908 In distribution
018.3611 In distribution
018.5312 In distribution
018.4910 In distribution
018.4810 In distribution
018.1110 In distribution
018.3308 In distribution
018.4016 In distribution
018.3414 In distribution
018.3914 In distribution
018.3012 In distribution
018.4414 In distribution
018.1910 In distribution
018.2514 In distribution
018.4513 In distribution
018.5316 In distribution
018.5412 In distribution
018.1714 In distribution
018.4109 In distribution
018.1312 In distribution
018.3915 In distribution
018.3210 In distribution
018.2809 In distribution
018.5016 In distribution
018.1314 In distribution
018.3411 In distribution
018.4911 In distribution
018.5211 In distribution
018.3313 In distribution
018.2508 In distribution
018.3316 In distribution
018.1107 In distribution
018.1711 In distribution
018.4115 In distribution
018.2709 In distribution
018.5411 In distribution
018.5410 In distribution
018.5310 In distribution
018.3910 In distribution
018.3716 In distribution
018.3209 In distribution
018.1707 In distribution
018.5012 In distribution
018.1916 In distribution
018.4813 In distribution
018.5311 In distribution
018.4010 In distribution
018.1307 In distribution
018.5015 In distribution
018.1912 In distribution
018.3315 In distribution
018.3614 In distribution
018.2515 In distribution
018.2710 In distribution
018.3015 In distribution
018.4610 In distribution
018.3510 In distribution
018.4509 In distribution
018.4311 In distribution
018.3909 In distribution
018.4514 In distribution
018.4615 In distribution
018.5108 In distribution
018.3913 In distribution
018.2715 In distribution
018.4510 In distribution
018.2814 In distribution
018.4112 In distribution
018.3815 In distribution
018.4611 In distribution
018.4511 In distribution
018.4409 In distribution
018.4614 In distribution
018.1907 In distribution
018.5109 In distribution
018.3509 In distribution
018.4316 In distribution
018.1716 In distribution
018.1715 In distribution
018.4410 In distribution
018.1111 In distribution
018.4708 In distribution
018.3508 In distribution
018.3515 In distribution
018.2611 In distribution
018.3610 In distribution
018.3812 In distribution
018.4209 In distribution
018.5408 In distribution
018.1313 In distribution
018.4808 In distribution
018.4008 In distribution
018.2912 In distribution

Showing 250 of 300 catalogue numbers.

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
K233947 2024-10-10
K231359 2023-06-09
K213641 2022-09-15
K192863 2020-08-26

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Cezanne II Lumbar Interbody Fusion Cage System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
CTL Medical Corporation 510(k) number 2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 39 units
CTL Medical Corporation 510(k) number 2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 39 units
CTL Medical Corporation 510(k) number 2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 45 units
CTL Medical Corporation 510(k) number 2019-08-21 Class II Device Design Reports received of the device fracturing during insertion. 46 units

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