Cezanne II Interbody Fusion System

CEZANNE-II DLIF Initial Distractor, 0° W19 x L60, H4mm, Short

Registry build 21.09.26
14manufacturers in China registered for this device type
162catalogue 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 Interbody Fusion 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 2025-06-04
Record revised 2026-04-30 (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
Distribution end date 2025-02-24

Catalogue Numbers

Catalogue numbers for Cezanne II Interbody Fusion System
Catalogue number Size Status
104.6514 In distribution
103.7209 In distribution
103.7114 In distribution
103.7032 In distribution
103.0009 In distribution
103.0011 In distribution
103.0115 In distribution
104.6460 In distribution
103.0015 In distribution
128.5229 In distribution
103.0006 In distribution
103.7250 In distribution
103.7211 In distribution
104.6264 In distribution
103.7214 In distribution
104.6236 In distribution
103.7106 In distribution
103.0116 In distribution
128.5429 In distribution
128.7295 In distribution
104.7033 In distribution
128.4029 In distribution
104.7034 In distribution
104.7711 In distribution
128.7294 In distribution
128.7132 In distribution
128.4036 In distribution
104.6024 In distribution
104.6358 In distribution
104.6810 In distribution
103.0114 In distribution
104.6052 In distribution
103.7035 In distribution
128.7131 In distribution
103.7115 In distribution
103.7110 In distribution
103.7111 In distribution
103.0008 In distribution
104.7712 In distribution
103.7107 In distribution
128.7134 In distribution
103.7108 In distribution
104.6262 In distribution
128.7136 In distribution
104.7031 In distribution
104.6050 In distribution
128.7133 In distribution
104.6464 In distribution
128.7135 In distribution
104.6510 In distribution
103.7216 In distribution
104.6258 In distribution
103.7256 In distribution
128.4229 In distribution
104.6022 In distribution
103.7116 In distribution
103.7112 In distribution
104.6230 In distribution
104.7142 In distribution
128.4236 In distribution
128.5230 In distribution
103.7248 In distribution
104.6044 In distribution
128.4234 In distribution
103.7207 In distribution
103.7022 In distribution
104.6130 In distribution
128.5228 In distribution
103.7031 In distribution
128.5330 In distribution
104.6764 In distribution
104.6762 In distribution
104.6362 In distribution
128.5328 In distribution
128.4230 In distribution
104.6020 In distribution
104.6232 In distribution
128.4034 In distribution
128.7292 In distribution
104.6042 In distribution
103.0013 In distribution
128.4232 In distribution
103.7113 In distribution
103.7215 In distribution
104.6164 In distribution
103.0106 In distribution
104.6158 In distribution
103.7252 In distribution
128.4228 In distribution
104.6128 In distribution
104.6814 In distribution
104.6808 In distribution
104.6812 In distribution
128.4231 In distribution
104.6760 In distribution
103.0014 In distribution
104.6134 In distribution
103.7253 In distribution
103.0110 In distribution
104.6364 In distribution
103.0107 In distribution
103.7251 In distribution
128.5428 In distribution
104.7700 In distribution
103.7210 In distribution
103.7255 In distribution
128.4031 In distribution
104.6048 In distribution
128.5430 In distribution
104.7032 In distribution
103.7247 In distribution
128.7130 In distribution
103.7249 In distribution
128.7129 In distribution
103.7109 In distribution
104.7035 In distribution
128.4233 In distribution
128.4032 In distribution
103.0109 In distribution
104.6018 In distribution
104.6038 In distribution
104.7141 In distribution
103.0112 In distribution
103.0111 In distribution
104.6040 In distribution
104.6056 In distribution
104.6160 In distribution
104.6260 In distribution
103.7023 In distribution
104.6162 In distribution
128.4033 In distribution
103.7034 In distribution
103.7212 In distribution
103.0010 In distribution
103.0007 In distribution
104.6462 In distribution
128.4030 In distribution
103.7033 In distribution
104.6508 In distribution
103.7025 In distribution
104.6054 In distribution
103.7021 In distribution
128.4035 In distribution
104.6512 In distribution
104.6234 In distribution
104.6360 In distribution
103.0108 In distribution
128.4028 In distribution
104.6132 In distribution
103.7105 In distribution
103.0016 In distribution
104.6228 In distribution
103.7254 In distribution
103.0113 In distribution
103.0012 In distribution
128.4235 In distribution
103.7208 In distribution
104.6026 In distribution
103.7213 In distribution
128.5329 In distribution
128.7128 In distribution
104.7750 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
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 Interbody Fusion 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