Verte-Stack®
Spacer 6287941 PSR LAT Ports 9X14X11
3manufacturers in China registered for this device type
1catalogue number
30510(k) clearances naming this product code
Who Else Makes It
Concentrated in Shanghai (1), Jiangsu (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
Record
| Listed by | Medtronic Sofamor Danek, Inc., United States |
|---|---|
| FDA product code | MQP |
| Device type | Spinal Vertebral Body Replacement Device |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3060 |
| 510(k) | K052931 |
| Record published | 2025-03-28 |
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 |
| Sizes | Height 14 mm; width 9 mm; depth 11 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 6287941 | Height 14.0 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| CoRoent | Nuvasive, Inc. | 1,514 |
| Capri™ Corpectomy Cage System | VB Spine LLC | 1,509 |
| Aleutian® Interbody Systems | VB Spine LLC | 1,189 |
| Fortify | Globus Medical, Inc. | 866 |
| Matrixx System | Nexxt Spine LLC | 748 |
| Ascend | Alphatec Spine, Inc. | 555 |
| Zavation VBR Trial | Zavation | 548 |
| Verte-Stack® Spinal System | Medtronic Sofamor Danek, Inc. | 484 |
| Timberline® Lateral Interbody Fusion System | Biomet Spine | 470 |
| Timberline Lateral Fusion System | Biomet Spine | 459 |
| Novel | Alphatec Spine, Inc. | 447 |
| Hawkeye™ Vertebral Body Replacement (VBR) | Choice Spine, LP | 368 |
Showing 12 of 683. All products under Spinal Vertebral Body Replacement Device
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K173125 | 2017-12-20 |
| K131888 | 2013-09-23 |
| K082112 | 2008-08-27 |
| K071033 | 2007-08-14 |
| K070173 | 2007-03-14 |
| K063491 | 2007-03-05 |
| K062427 | 2006-09-12 |
| K062073 | 2006-08-14 |
| K061938 | 2006-08-09 |
| K060719 | 2006-04-14 |
| K052931 | 2005-11-16 |
| K051105 | 2005-06-09 |
| K043566 | 2005-01-07 |
| K043561 | 2004-12-29 |
| K041197 | 2004-08-09 |
| K033926 | 2004-07-07 |
| K041556 | 2004-07-01 |
| K041452 | 2004-06-24 |
| K040536 | 2004-05-05 |
| K040422 | 2004-03-19 |
| K040167 | 2004-02-18 |
| K031780 | 2003-07-30 |
| K030735 | 2003-04-18 |
| K030736 | 2003-04-02 |
| K030601 | 2003-03-25 |
| K024049 | 2003-02-26 |
| K023570 | 2002-11-19 |
| K021791 | 2002-08-26 |
| K011406 | 2001-12-27 |
| K010930 | 2001-10-24 |
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.