SpaceFlex Hip Trial 900202
by G21 SRL
SpaceFlex Hip Trial 900202 is a Class I device made by G21 SRL, listed in FDA GUDID since 10 Oct 2024 (UDI-DI 08058964727879), 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 | Number08058964727879 | Date10 Oct 2024 | StatusListed |
Official records
- AccessGUDID record 08058964727879
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- SpaceFlex Hip Trial
- Generic name
- Hip revision prosthesis trial
- Model / reference
- 900202
- Primary DI / UDI-DI
- 08058964727879
- FDA product code
- HWT
- GMDN term
- Hip revision prosthesis trial
- Device class
- Class I
- Regulation number
- 888.4800
- GUDID distribution status
- In Commercial Distribution
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