Vertestack® Spinal System
Spacer X1205304 Titanium IMP 13MM X 30MM
3manufacturers in China registered for this device type
41catalogue numbers in this listing
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) | K062073 |
| Record published | 2015-07-08 |
| Record revised | 2025-07-14 (version 5) |
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 |
| Distribution end date | 2018-10-08 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 636853 | In distribution | |
| X1205304 | In distribution | |
| 3393320 | LG 8DEG 20mm, Dia 30mm x 24mm | In distribution |
| X1205303 | In distribution | |
| X0905249 | In distribution | |
| 3393314 | LG 8 DEG 14mm, Dia 30mm x 24mm | In distribution |
| X1205302 | In distribution | |
| X0905245 | In distribution | |
| 3393420 | LG 12DEG 20mm, Dia 30mm x 24mm | In distribution |
| X1205306 | In distribution | |
| 636132 | In distribution | |
| 3393418 | LG 12DEG 18mm, Dia 30mm x 24mm | In distribution |
| X1205301 | In distribution | |
| 636653 | In distribution | |
| X1205305 | In distribution | |
| 3393318 | LG 8DEG 18mm, Dia 30mm x 24mm | In distribution |
| 3393412 | LG 12DEG 12mm, Dia 30mm x 24mm | In distribution |
| X1205300 | In distribution | |
| 636532 | In distribution | |
| 636053 | In distribution | |
| 636953 | In distribution | |
| X0905253 | In distribution | |
| 636153 | In distribution | |
| X0905255 | In distribution | |
| 636553 | In distribution | |
| X0905257 | In distribution | |
| 9193615 | In distribution | |
| 636753 | In distribution | |
| 636832 | In distribution | |
| 3393416 | LG 12DEG 16mm, Dia 30mm x 24mm | In distribution |
| 636253 | In distribution | |
| 3393414 | LG 12DEG 14mm, Dia 30mm x 24mm | In distribution |
| X0504168 | 16×22 (mm) | In distribution |
| 636032 | In distribution | |
| X1205299 | In distribution | |
| X1205298 | In distribution | |
| 636732 | In distribution | |
| 3393316 | LG 8 DEG 16mm, Dia 30mm x 24mm | In distribution |
| 636932 | In distribution | |
| 636632 | In distribution | |
| 636232 | Withdrawn |
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.