Legion E0017131-1
Legion E0017131-1 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 21 Sep 2020 (UDI-DI 00885556794494), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00885556794494 | Date21 Sep 2020 | StatusListed |
Official records
- AccessGUDID record 00885556794494
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Legion
- Generic name
- Bone approximation clamp
- Model / Ref / Catalog
- E0017131-1
- Primary DI / UDI-DI
- 00885556794494
- FDA product code
- HXD
- GMDN term
- Bone approximation clamp
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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