Bone Fixation Wire
510(k) K882967
Bone Fixation Wire is a Class II device made by Baxter Healthcare Corp, cleared under FDA 510(k) K882967 on 30 Sep 1988, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK882967 | Date30 Sep 1988 | StatusActive |
Official records
- FDA 510(k) database K882967
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JDQ
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3010
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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