4WEB Cervical Spine Truss System Stand-Alone
by 4WEB EU B.V. Netherlands EUDAMED510(k)GUDID
Ref CSTS-SA-MD0011-SP510(k) K253200
Product code OVEEMDN P09070101
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00812998039227 | Date27 Jan 2026 | StatusActive |
| United States | FDA 510(k)SESE 510(k) | NumberK253200 | Date11 Dec 2025 | StatusActive |
| United States | GUDID listing GUDID | Number00812998039227 | Date11 Oct 2019 | StatusIn distribution |
Coverage
- Active
- Expiring (legacy directive)
- Not covered
- United States
- European Union
Specification
- Trade Name
- 4WEB Cervical Spine Truss System Stand-Alone EUDAMED4WEB Medical GUDID
- Generic Name
- Metallic spinal interbody fusion cage
- Device Name
- Csts Stand Alone Ifd, 17W X 14D X 11H, 0 Deg
- Model / Ref / Catalog
- CSTS-SA-MD0011-SP
- Primary DI / UDI-DI
- 00812998039227
- Basic UDI-DI
- B-00812998039227
- FDA Product Code
- OVE
- EMDN Code
- P09070101 Spinal cages
- GMDN Term
- Metallic spinal interbody fusion cage
- Device Class
- Class IIb EUDAMEDClass II GUDID
- Regulation Number
- 888.3080
- Market of Registration
- Netherlands
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Conditional
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIb | Class II |
Manufacturer details
- EUDAMED SRN
- NL-MF-000010951
- FDA applicant
- 4Web Medical, Inc.
Other devices from 4WEB EU B.V.
Properties & raw data
Show properties, registry sources and raw records
Other properties (16)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No
Sources (3)
- EUDAMED dca8bd59-774f-46f8-bb96-97573e22404c
- FDA UDI 0b5be9f1-6f6d-4c76-8aaf-5eb86ba5a903
- FDA 510(k) K253200