Cannulated Screws 71177123
Cannulated Screws 71177123 is a Class II device made by Smith & Nephew, Inc., cleared under FDA 510(k) K123055 on 25 Jan 2013 and listed in FDA GUDID since 28 Sep 2015 (UDI-DI 00885556016237), 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 | Number00885556016237 | Date28 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK123055 | Date25 Jan 2013 | StatusActive |
Official records
- AccessGUDID record 00885556016237
- FDA 510(k) database K123055
Across registries
- FDA 510(k) K123055 decided 25 Jan 2013 Active
- FDA GUDID UDI-DI 00885556016237 listed 28 Sep 2015 Listed
Timeline
- Cleared FDA 510(k) K123055
- Listed FDA GUDID 00885556016237
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cannulated Screws
- Generic name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / Ref / Catalog
- 71177123
- Primary DI / UDI-DI
- 00885556016237
- 510(k) Number
- FDA product code
- HRS
- GMDN term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution