Ballista Percutaneous Pedicle Screw System
27 catalogue numbers from 2000-3540, listed by Biomet Spine, United States, under Appliance, Fixation, Spinal Intervertebral Body. 14 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 74 |
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou | Guangdong | Contract manufacturer | 62 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| APS Materials Suzhou | Suzhou | Jiangsu | Contract manufacturer | 18 |
| Zibo Dante Co., Ltd. | Zibo | Shandong | Contract manufacturer | 17 |
| Shanghai JPY ION-Tech Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 70 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
| Johnson & Johnson Medical (Depuy – Suzhou) Ltd. | Suzhou | Jiangsu | Manufacturer | 34 |
| Double Medical Technology Inc. | Xiamen | Fujian | Contract manufacturer | 14 |
Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body
Record
| Listed by | Biomet Spine, United States |
|---|---|
| FDA product code | KWQ |
| Device type | Appliance, Fixation, Spinal Intervertebral Body |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3060 |
| Record published | 2015-10-24 |
| Record revised | 2025-07-02 (version 6) |
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, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 2000-3540 | 7.5X 40MM CANNULATED SCREW | In distribution |
| 2000-3335E | 5.5 X 35MM CANNULATED SCREW | In distribution |
| 2000-3630 | 8.5X 30MM CANNULATED SCREW | In distribution |
| 2000-3620 | 8.5X 20MM CANNULATED SCREW | In distribution |
| 2000-3370 | 5.5X 70MM CANNULATED SCREW | In distribution |
| 2000-5235 | 35MM PERCUTANEOUS ROD | In distribution |
| 2000-3460E | 6.5 X 60MM CANNULATED SCREW | In distribution |
| 2000-3775 | 9.5X 75MM CANNULATED SCREW | In distribution |
| 2000-3490 | 6.5X 90MM CANNULATED SCREW | In distribution |
| 2000-3555 | 7.5X 55MM CANNULATED SCREW | In distribution |
| 2000-3560 | 7.5X 60MM CANNULATED SCREW | In distribution |
| 2000-3450E | 6.5 X 50MM CANNULATED SCREW | In distribution |
| 2000-3330 | 5.5X 30MM CANNULATED SCREW | In distribution |
| 2000-3345E | 5.5 X 45MM CANNULATED SCREW | In distribution |
| 2000-3825 | 10.5X 25MM CANNULATED SCREW | In distribution |
| 2000-3875 | 10.5X 75MM CANNULATED SCREW | In distribution |
| 2000-3790 | 9.5X 90MM CANNULATED SCREW | In distribution |
| 2000-3785 | 9.5X 85MM CANNULATED SCREW | In distribution |
| 2000-3365 | 5.5X 65MM CANNULATED SCREW | In distribution |
| 2000-3599 | 7.5X 100MM CANNULATED SCREW | In distribution |
| 2000-3795 | 9.5X 95MM CANNULATED SCREW | In distribution |
| 2000-5255 | 55MM PERCUTANEOUS ROD | In distribution |
| 2000-5265 | 65MM PERCUTANEOUS ROD | In distribution |
| 2000-3465 | 6.5X 65MM CANNUALTED SCREW | In distribution |
| 2000-3640 | 8.5X 40MM CANNULATED SCREW | In distribution |
| 2000-3870 | 10.5X 70MM CANNULATED SCREW | In distribution |
| 2000-3380 | 5.5X 80MM CANNULATED SCREW | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ReLine | Nuvasive, Inc. | 2,998 |
| CD Horizon® Spinal System | Medtronic Sofamor Danek, Inc. | 2,568 |
| Creo | Globus Medical, Inc. | 1,765 |
| AccelFix Spinal Fixation System | L&K Biomed Co., Ltd. | 1,755 |
| Ozark Cervical Plate System | VB Spine LLC | 1,460 |
| Sirion | Astura Medical | 1,246 |
| Apex Spine System | Spinecraft LLC | 1,187 |
| AnyPlus Spinal Fixation System | GS Medical Co., Ltd. | 986 |
| Astra Spine System | Spinecraft LLC | 970 |
| Zavation | Zavation | 966 |
| ACP | Nuvasive, Inc. | 918 |
| Polaris™ 5.5 Spinal System | Biomet Spine | 877 |
Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K103393 | 2011-02-02 |
| K080646 | 2008-05-02 |
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.