Cezanne II Lumbar Interbody Fusion Cage System
CEZANNE-II™ DLIF PEEK Cage, 12Deg., W19 x L40, H16mm
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.
| 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
| 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
| 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 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 | |
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| 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 | |
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| 018.3916 | In distribution | |
| 018.3713 | In distribution | |
| 018.2616 | In distribution | |
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| 018.4108 | In distribution | |
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| 018.2815 | In distribution | |
| 018.3412 | In distribution | |
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| 018.4909 | In distribution | |
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| 018.1913 | In distribution | |
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| 018.3715 | In distribution | |
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| 018.4816 | In distribution | |
| 018.2812 | In distribution | |
| 018.3513 | In distribution | |
| 018.5416 | In distribution | |
| 018.4715 | In distribution | |
| 018.3811 | In distribution | |
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| 018.5309 | In distribution | |
| 018.4815 | In distribution | |
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| 018.1915 | In distribution | |
| 018.4110 | In distribution | |
| 018.1713 | In distribution | |
| 018.5113 | In distribution | |
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| 018.3612 | In distribution | |
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| 018.1107 | In distribution | |
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| 018.4115 | In distribution | |
| 018.2709 | In distribution | |
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| 018.3209 | In distribution | |
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| 018.3315 | In distribution | |
| 018.3614 | In distribution | |
| 018.2515 | In distribution | |
| 018.2710 | In distribution | |
| 018.3015 | In distribution | |
| 018.4610 | In distribution | |
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| 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 | |
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| 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 | |
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| 018.4209 | In distribution | |
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Showing 250 of 300 catalogue numbers.
Same 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
| 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.
| 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.
| 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.