X-Core
XCMini Endcap 19x16mm 4° Kyp Top Ang Ø14
3manufacturers in China registered for this device type
270catalogue numbers in this listing
6510(k) clearances naming this product code
1recall
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 | Nuvasive, Inc., United States |
|---|---|
| FDA product code | MQP |
| Device type | Spinal Vertebral Body Replacement Device |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3060 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K090176 |
| Record published | 2015-10-24 |
| Record revised | 2025-06-11 (version 9) |
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, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 5964960 | In distribution | |
| 5962526 | In distribution | |
| 6538318 | In distribution | |
| 5962366 | In distribution | |
| 7262604 | In distribution | |
| 7180121A | In distribution | |
| 6591011 | In distribution | |
| 5163014P2 | In distribution | |
| 7220055 | In distribution | |
| 7220079A | In distribution | |
| 7180055 | In distribution | |
| 6537225 | In distribution | |
| 7160063 | In distribution | |
| 7481020 | In distribution | |
| 6183004 | In distribution | |
| 6535541 | In distribution | |
| 6537226 | In distribution | |
| 5962253P2 | In distribution | |
| 7220033A | In distribution | |
| 6225008 | In distribution | |
| 7180041 | In distribution | |
| 7222204 | In distribution | |
| 7160025 | In distribution | |
| 6184008 | In distribution | |
| 6223004 | In distribution | |
| 6184004 | In distribution | |
| 6533341 | In distribution | |
| 7491855 | In distribution | |
| 6225000 | In distribution | |
| 6539018 | In distribution | |
| D7225100 | In distribution | |
| 6535461 | In distribution | |
| 7220016 | In distribution | |
| 5964172P2 | In distribution | |
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| 5964746 | In distribution | |
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| 7160025P2 | In distribution | |
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| 6225012 | In distribution | |
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| 6538250 | In distribution | |
| 6226008 | In distribution | |
| 6533331 | In distribution | |
| 6533151 | In distribution | |
| 6536130 | In distribution | |
| 7220121 | In distribution |
Showing 250 of 270 catalogue numbers.
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 |
|---|---|
| K142205 | 2015-02-20 |
| K090176 | 2009-04-27 |
| K052210 | 2005-12-12 |
| K043405 | 2005-02-07 |
| K032476 | 2003-11-13 |
| K023319 | 2003-03-04 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Nuvasive, Inc. | 510(k) number | 2022-11-10 | Class II | Device Design | Potential that insert will be unable to disengage from the vertebral body replacement device/implant | 2,031 devices |
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.