Kirschner Wire K10 NS151
by IN2BONES
Kirschner Wire K10 NS151 is a Class I device made by IN2BONES, cleared under FDA 510(k) K153204 on 1 Feb 2016 and listed in FDA GUDID since 4 Jun 2020 (UDI-DI 03760225717417), 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 | Number03760225717417 | Date4 Jun 2020 | StatusListed |
| United States | FDA 510(k) | NumberK153204 | Date1 Feb 2016 | StatusActive |
Official records
- AccessGUDID record 03760225717417
- FDA 510(k) database K153204
Across registries
- FDA 510(k) K153204 decided 1 Feb 2016 Active
- FDA GUDID UDI-DI 03760225717417 listed 4 Jun 2020 Listed
Timeline
- Cleared FDA 510(k) K153204
- Listed FDA GUDID 03760225717417
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kirschner Wire
- Generic name
- Orthopaedic bone pin, non-bioabsorbable
- Model / Ref / Catalog
- K10 NS151
- Primary DI / UDI-DI
- 03760225717417
- 510(k) Number
- FDA product code
- FZX, HTY, JDW
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class I
- Regulation number
- 878.4800, 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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