Transverse Traction Assembly
by Zimmer, Inc.
510(k) K790238
Transverse Traction Assembly is a Class II device made by Zimmer, Inc., cleared under FDA 510(k) K790238 on 12 Feb 1979, 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 | NumberK790238 | Date12 Feb 1979 | StatusActive |
Official records
- FDA 510(k) database K790238
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KWP
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3050
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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