K-Wire
by Onyx Medical Corp. 510(k)
Active
510(k) K903264
Overview
The K-Wire is an orthopedic device, substantially equivalent to other devices in its class. It is made of 316L Stainless Steel and is available in various configurations, including single ended, double ended, and threaded trocar points, in a range of diameters and lengths.
The K-Wire is supplied in multiple sizes and is used in orthopedic procedures. It has been cleared by the FDA with a 510(k) number of K903264 and a product code of HTY. The device is manufactured by Onyx Medical Corp. and has been assigned a decision description of Substantially Equivalent.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK903264 | Date30 Jul 1990 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- HTY
- Device Class
- Class II
- Regulation
- 21 CFR Part 888.3040
- Advisory Committee
- Orthopedic
- FDA Decision
- SESE Substantially Equivalent
Other devices from Onyx Medical LLC
Questions
What is the K-Wire used for?
The K-Wire is used in orthopedic procedures, and is available in various configurations, including single ended, double ended, and threaded trocar points.
What materials is the K-Wire made of?
The K-Wire is made of 316L Stainless Steel, a durable and corrosion-resistant material.
Is the K-Wire available in different sizes?
Yes, the K-Wire is supplied in multiple sizes and diameters to accommodate various orthopedic procedures and patient needs.