Mectalif Oblique
Oblique Interbody Fusion Device 12x40x15 L10°
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 | Medacta International SA, Switzerland |
|---|---|
| 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, Private-label distributor, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K133192 |
| Record published | 2014-11-18 |
| Record revised | 2025-07-14 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 03.26.044 | In distribution | |
| 03.26.034 | In distribution | |
| 03.26.089 | In distribution | |
| 03.26.003 | In distribution | |
| 03.26.033 | In distribution | |
| 03.26.028 | In distribution | |
| 03.26.005 | In distribution | |
| 03.26.004 | In distribution | |
| 03.26.095 | In distribution | |
| 03.26.102 | In distribution | |
| 03.26.010 | In distribution | |
| 03.26.117 | In distribution | |
| 03.26.113 | In distribution | |
| 03.26.118 | In distribution | |
| 03.26.104 | In distribution | |
| 03.26.068 | In distribution | |
| 03.26.055 | In distribution | |
| 03.26.017 | In distribution | |
| 03.26.030 | In distribution | |
| 03.26.009 | In distribution | |
| 03.26.006 | In distribution | |
| 03.26.097 | In distribution | |
| 03.26.066 | In distribution | |
| 03.26.120 | In distribution | |
| 03.26.036 | In distribution | |
| 03.26.111 | In distribution | |
| 03.26.087 | In distribution | |
| 03.26.021 | In distribution | |
| 03.26.060 | In distribution | |
| 03.26.049 | In distribution | |
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| 03.26.114 | In distribution | |
| 03.26.084 | In distribution | |
| 03.26.057 | In distribution | |
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| 03.26.050 | In distribution | |
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| 03.26.061 | In distribution | |
| 03.26.073 | In distribution | |
| 03.26.069 | In distribution | |
| 03.26.067 | In distribution | |
| 03.26.053 | In distribution | |
| 03.26.092 | In distribution | |
| 03.26.015 | In distribution | |
| 03.26.070 | In distribution | |
| 03.26.123 | In distribution | |
| 03.26.035 | In distribution | |
| 03.26.019 | In distribution | |
| 03.26.012 | In distribution | |
| 03.26.040 | In distribution | |
| 03.26.081 | In distribution | |
| 03.26.018 | In distribution | |
| 03.26.099 | In distribution | |
| 03.26.029 | In distribution | |
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| 03.26.072 | In distribution | |
| 03.26.051 | In distribution | |
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| 03.26.109 | In distribution | |
| 03.26.076 | In distribution | |
| 03.26.054 | In distribution | |
| 03.26.038 | In distribution | |
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| 03.26.086 | In distribution | |
| 03.26.079 | In distribution | |
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| 03.26.121 | In distribution | |
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| 03.26.056 | In distribution | |
| 03.26.107 | In distribution | |
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| 03.26.042 | In distribution | |
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| 03.26.096 | In distribution | |
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| 03.26.025 | In distribution | |
| 03.26.027 | In distribution | |
| 03.26.058 | In distribution | |
| 03.26.063 | In distribution | |
| 03.26.078 | In distribution | |
| 03.26.052 | In distribution | |
| 03.26.039 | In distribution | |
| 03.26.032 | In distribution | |
| 03.26.103 | In distribution | |
| 03.26.037 | In distribution | |
| 03.26.047 | In distribution | |
| 03.26.091 | In distribution | |
| 03.26.090 | In distribution | |
| 03.26.112 | In distribution | |
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| 03.26.026 | In distribution | |
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| 03.26.075 | In distribution | |
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| 03.26.122 | In distribution | |
| 03.26.002 | In distribution | |
| 03.26.093 | In distribution |
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 |
|---|---|
| K133192 | 2014-01-30 |
| K131671 | 2013-07-05 |
| K110927 | 2011-06-13 |
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.