InterSpace Hip Trial SPC90Z1
by Tecres
InterSpace Hip Trial SPC90Z1 is a Class I device made by Tecres, listed in FDA GUDID since 23 Sep 2022 (UDI-DI 08031497002873), 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 | Number08031497002873 | Date23 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 08031497002873
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- InterSpace Hip Trial
- Generic name
- Hip revision prosthesis trial
- Model / reference
- SPC90Z1
- Primary DI / UDI-DI
- 08031497002873
- FDA product code
- HWT
- GMDN term
- Hip revision prosthesis trial
- Device class
- Class I
- Regulation number
- 888.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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