P-Lift®
P-LIFT, Straight, CONED, 8W X 27L X 11H
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 | Spinefrontier, Inc., United States |
|---|---|
| FDA product code | MAX |
| Device type | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3080 |
| 510(k) | K111553 |
| Record published | 2016-04-15 |
| Record revised | 2020-02-24 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| Sizes | Length 22 to 30 mm; width 8 to 9 mm; height 8 to 14 mm |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 01-06014-11 | Length 27 mm | In distribution |
| 01-06021-10 | Height 10 mm | In distribution |
| 01-06013-13 | Width 8 mm | In distribution |
| 01-06013-10 | Height 10 mm | In distribution |
| 01-06014-14 | Height 14 mm | In distribution |
| 01-06021-08 | Length 27 mm | In distribution |
| 01-06013-12 | Width 8 mm | In distribution |
| 01-06013-09 | Length 24 mm | In distribution |
| 01-06020-10 | Height 10 mm | In distribution |
| 01-06014-08 | Length 27 mm | In distribution |
| 13-06000 | In distribution | |
| 01-06013-11 | Height 11 mm | In distribution |
| 01-06021-09 | Width 8 mm | In distribution |
| 01-06014-09 | Height 9 mm | In distribution |
| 01-06013-08 | Length 24 mm | In distribution |
| 01-06022-11 | Width 8 mm | In distribution |
| 01-06013-14 | Height 14 mm | In distribution |
| 01-06020-12 | Width 9 mm | In distribution |
| 01-06020-13 | Width 9 mm | In distribution |
| 01-06014-13 | Width 8 mm | In distribution |
| 01-06020-09 | Height 9 mm | In distribution |
| 01-06014-12 | Length 27 mm | In distribution |
| 01-06022-10 | Height 10 mm | In distribution |
| 01-06021-12 | Height 12 mm | In distribution |
| 01-06022-14 | Length 30 mm | In distribution |
| 01-06020-08 | Length 24 mm | In distribution |
| 01-06022-09 | Height 9 mm | In distribution |
| 01-06020-11 | Width 9 mm | In distribution |
| 01-06021-14 | Length 27 mm | In distribution |
| 01-06022-12 | Width 8 mm | In distribution |
| 01-06022-08 | Width 8 mm | In distribution |
| 01-06021-11 | Width 8 mm | In distribution |
| 01-06022-13 | Height 13 mm | In distribution |
| 01-06014-10 | Height 10 mm | In distribution |
| 01-06020-14 | Height 14 mm | In distribution |
| 01-06021-13 | Length 27 mm | In distribution |
| 01-06000-14 | Width 8 mm | 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 |
|---|---|
| K193106 | 2020-06-19 |
| K142504 | 2015-05-13 |
| K111553 | 2011-09-28 |
| K092815 | 2010-06-30 |
| K091638 | 2009-09-14 |
| K072289 | 2007-11-01 |
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.