Xpand 116.102
Xpand 116.102 is a Class II device made by Globus Medical, Inc., cleared under FDA 510(k) K050850 on 26 May 2005 and listed in FDA GUDID since 9 Oct 2015 (UDI-DI 00849044022469), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00849044022469 | Date9 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK050850 | Date26 May 2005 | StatusActive |
Official records
- AccessGUDID record 00849044022469
- FDA 510(k) database K050850
Across registries
- FDA 510(k) K050850 decided 26 May 2005 Active
- FDA GUDID UDI-DI 00849044022469 listed 9 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K050850
- Listed FDA GUDID 00849044022469
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Xpand
- Generic name
- Vertebral body prosthesis
- Model / reference
- 116.102
- Primary DI / UDI-DI
- 00849044022469
- 510(k) Number
- FDA product code
- MQP
- GMDN term
- Vertebral body prosthesis
- Device class
- Class II
- Regulation number
- 888.3060
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Height — 18 MillimeterWidth — 14 MillimeterDepth — 12 Millimeter
Similar devices
Other devices filed under FDA product code MQP (SPINAL VERTEBRAL BODY REPLACEMENT DEVICE).
- T2 XVBR 1.5 SPINAL SYSTEM by MEDTRONIC SOFAMOR DANEK, INC.
- BENGAL 177308411 by Depuy Spine, Inc.
- KONG-C VBR System, Trial End Plate, 0° / 14 x 13 mm 43-140 by icotec AG
- AESCULAP HYDROLIFT VBR SYSTEM by Aesculap Implant Systems, Inc.
- STRYKER SPINE AVS ASL PEEK SPACER by Stryker Spine
- CONCORDE 187823409 by MEDOS INTERNATIONAL SARL
- PYRAMESH® Implant System 905-139 by MEDTRONIC SOFAMOR DANEK, INC.
- QUANTUM VERTEBRAL BODY REPLACEMENT by Quantum Orthopedics, Inc.
- KONG-TL VBR System, Adapter for Expansion Handle 44-077 by icotec AG
- GRAFTCAGE TLX by Osteotech, Inc.