Orthros Cc-117-50
Orthros Cc-117-50 is a Class I device made by Camber Spine Technologies, listed in FDA GUDID since 25 Nov 2022 (UDI-DI B030CC117500), 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 | NumberB030CC117500 | Date25 Nov 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Orthros
- Generic name
- Orthopaedic implantation sleeve, reusable
- Model / reference
- CC-117-50
- Primary DI / UDI-DI
- B030CC117500
- FDA product code
- LXH
- GMDN term
- Orthopaedic implantation sleeve, reusable
- Device class
- Class I
- Regulation number
- 888.4540
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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