Carpenter Bone Clamp
510(k) K770118
Carpenter Bone Clamp is a medical device (FDA Class I; FDA product code HXD, Clamp) made by Stryker Corp., cleared under FDA 510(k) K770118 on 26 Jan 1977, 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 | NumberK770118 | Date26 Jan 1977 | StatusActive |
Official records
- FDA 510(k) database K770118
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HXD
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4800
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code HXD (Clamp).
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- GIZMO TOWEL CLAMP by Hemoy, Inc.