Solution Hip
by Depuy, Inc. 510(k)
Active
510(k) K941942
Overview
The Solution Hip is a hip replacement implant designed for revision surgery. It features press-fit fixation, a cylindrical design, a standard collar, and a bullet tip with one lateral hole.
This device is supplied as a single-use implant and is not MRI safe. It is authorized under FDA 510K clearance with product code LZO and K-number K941942.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK941942 | Date12 Jul 1994 | 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- Withdrawn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
- LZO
- Device Class
- Class II
- Regulation
- 21 CFR Part 888.3353
- Advisory Committee
- Orthopedic
- FDA Decision
- SESE Substantially Equivalent
Other devices from Depuy, Inc.
Questions
What is the Solution Hip implant used for?
The Solution Hip is a hip replacement implant specifically designed for revision surgery. It features press-fit fixation, a cylindrical design, a standard collar, and a bullet tip with one lateral hole to facilitate surgical procedures.
How is the Solution Hip supplied and can it be reused?
The Solution Hip is supplied as a single-use implant, meaning it is designed for one surgical procedure only and should not be reused for patient safety reasons.
Is the Solution Hip MRI safe?
No, the Solution Hip implant is not MRI safe, meaning patients with this implant should avoid MRI scans as it may interfere with the imaging process or pose safety risks.
What regulatory approvals does the Solution Hip have?
The Solution Hip is authorized under FDA 510K clearance with product code LZO and K-number K941942, indicating it has been determined to be substantially equivalent to existing devices.