K-Wire 7332-73D
K-Wire 7332-73D is a Class II device made by Koros USA, Inc., cleared under FDA 510(k) K120590 on 7 May 2013 and listed in FDA GUDID since 31 Jan 2022 (UDI-DI 10840199500014), 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 | Number10840199500014 | Date31 Jan 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK120590 | Date7 May 2013 | StatusActive |
Official records
- AccessGUDID record 10840199500014
- FDA 510(k) database K120590
Across registries
- FDA 510(k) K120590 decided 7 May 2013 Active
- FDA GUDID UDI-DI 10840199500014 listed 31 Jan 2022 Listed
Timeline
- Cleared FDA 510(k) K120590
- Listed FDA GUDID 10840199500014
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- K-Wire
- Generic name
- Nerve-locating system probe, single-use
- Model / reference
- 7332-73D
- Primary DI / UDI-DI
- 10840199500014
- 510(k) Number
- FDA product code
- GXZ
- GMDN term
- Nerve-locating system probe, single-use
- Device class
- Class II
- Regulation number
- 882.1350
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Nerve-locating system probe, single-use.