ProLift
Static Expandable Cage Trial, 12mm x 28mm x 12mm, 12 Degree
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 | Life 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, Manufacturer |
| 510(k) | K190488 |
| Record published | 2019-11-19 |
| Record revised | 2025-07-14 (version 3) |
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 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 151-607 | In distribution | |
| 151-628 | In distribution | |
| 58-0828-1508 | In distribution | |
| 58-0828-0813K | In distribution | |
| 151-479 | In distribution | |
| 58-1840-0710 | In distribution | |
| L151-1050 | In distribution | |
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| L151-219 | In distribution | |
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| 151-811 | In distribution | |
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| L149-2168 | In distribution | |
| 58-0828-1016K | In distribution | |
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| 58-2655-1512 | In distribution | |
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| 58-0828-0710K | In distribution | |
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| L114-965-2 | In distribution | |
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| 58-1228-0813K | In distribution | |
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| L114-966-2 | In distribution | |
| L151-882 | In distribution | |
| 58-1032-1510K | In distribution | |
| 151-658 | In distribution | |
| L114-963-1 | In distribution | |
| L114-964-1 | In distribution | |
| L151-234 | In distribution |
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 |
|---|---|
| K261430 | 2026-07-28 |
| K260837 | 2026-05-12 |
| K253748 | 2026-01-23 |
| K251502 | 2025-07-07 |
| K250373 | 2025-04-09 |
| K243668 | 2025-01-23 |
| K242826 | 2024-10-08 |
| K232611 | 2023-11-30 |
| K223430 | 2023-05-04 |
| K221806 | 2022-12-05 |
| K213417 | 2022-09-29 |
| K212520 | 2021-10-08 |
| K210061 | 2021-04-30 |
| K203361 | 2021-03-17 |
| K201721 | 2020-09-04 |
| K201500 | 2020-08-04 |
| K193521 | 2020-02-06 |
| K193258 | 2020-01-31 |
| K190721 | 2019-11-14 |
| K190488 | 2019-07-23 |
| K191005 | 2019-06-13 |
| K181625 | 2018-12-11 |
| K182470 | 2018-11-26 |
| K172105 | 2018-02-02 |
| K173182 | 2017-12-20 |
| K170919 | 2017-08-03 |
| K153400 | 2016-03-07 |
| K133717 | 2014-09-19 |
| K131077 | 2013-07-17 |
| K130630 | 2013-06-13 |
| K121116 | 2012-05-08 |
| K111569 | 2011-07-06 |
| K080411 | 2008-05-15 |
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.