Triway N20 ST722
by IN2BONES
Triway N20 ST722 is a Class II device made by IN2BONES, cleared under FDA 510(k) K173811 on 15 Mar 2018 and listed in FDA GUDID since 13 Dec 2024 (UDI-DI 03701337615598), 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 | Number03701337615598 | Date13 Dec 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173811 | Date15 Mar 2018 | StatusActive |
Official records
- AccessGUDID record 03701337615598
- FDA 510(k) database K173811
Across registries
- FDA 510(k) K173811 decided 15 Mar 2018 Active
- FDA GUDID UDI-DI 03701337615598 listed 13 Dec 2024 Listed
Timeline
- Cleared FDA 510(k) K173811
- Listed FDA GUDID 03701337615598
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Triway
- Generic name
- Orthopaedic bone screw (non-sliding)
- Model / Ref / Catalog
- N20 ST722
- Primary DI / UDI-DI
- 03701337615598
- 510(k) Number
- FDA product code
- HWC
- GMDN term
- Orthopaedic bone screw (non-sliding)
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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