Su-Veid 18103300
Su-Veid 18103300 is a Class II device made by Angie Technologies Ltd, cleared under FDA 510(k) K993995 on 14 Feb 2000 and listed in FDA GUDID since 23 May 2021 (UDI-DI 07290018896235), 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 | Number07290018896235 | Date23 May 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK993995 | Date14 Feb 2000 | StatusActive |
Official records
- AccessGUDID record 07290018896235
- FDA 510(k) database K993995
Across registries
- FDA 510(k) K993995 decided 14 Feb 2000 Active
- FDA GUDID UDI-DI 07290018896235 listed 23 May 2021 Listed
Timeline
- Cleared FDA 510(k) K993995
- Listed FDA GUDID 07290018896235
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Su-Veid
- Generic name
- Rib/rib cage internal fixation/bracing system bracing bar
- Model / Ref / Catalog
- 18103300
- Primary DI / UDI-DI
- 07290018896235
- 510(k) Number
- FDA product code
- FRF
- GMDN term
- Rib/rib cage internal fixation/bracing system bracing bar
- Device class
- Class II
- Regulation number
- 880.5045
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
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