Kirschner wire K10 NS250
by IN2BONES
Kirschner wire K10 NS250 is a Class II device made by IN2BONES, cleared under FDA 510(k) K153204 on 1 Feb 2016 and listed in FDA GUDID since 18 Mar 2016 (UDI-DI 03760225710791), 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 | Number03760225710791 | Date18 Mar 2016 | StatusListed |
| United States | FDA 510(k) | NumberK153204 | Date1 Feb 2016 | StatusActive |
Official records
- AccessGUDID record 03760225710791
- FDA 510(k) database K153204
Across registries
- FDA 510(k) K153204 decided 1 Feb 2016 Active
- FDA GUDID UDI-DI 03760225710791 listed 18 Mar 2016 Listed
Timeline
- Cleared FDA 510(k) K153204
- Listed FDA GUDID 03760225710791
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- Withdrawn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 NS250
- Primary DI / UDI-DI
- 03760225710791
- 510(k) Number
- FDA product code
- HTY, FZX, JDW
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040, 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 250 MillimeterOuter Diameter — 2.5 Millimeter
Similar devices in this category
Other devices filed under Orthopaedic bone pin, non-bioabsorbable.
- XtraFix® 00-5214-030-20 by Zimmer, Inc.
- NA NK 0014-08 by aap Implantate AG
- NA NK 0025-28 by aap Implantate AG
- Affixus® Natural Nail® 110035666 by Zimmer, Inc.
- Pin S581030065 by Tianjin Zhengtian Medical Instrument Co., Ltd.
- ZİMED MEDİKAL SANAYİ VE TİCARET LİMİTED ŞİRKETİ 2932-4018 by Zimed Medikal Sanayi ve Ticaret Limited Şirketi
- 690035 by Stryker GmbH
- 6007-004-100 by Stryker Leibinger
- IlluminOss CT-0301 by IlluminOss Medical