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hg multilock hip prosthesis w tinidium surface
Zimmer
Summary: The HG Multilock Hip Prosthesis by Zimmer is a hip replacement device used in orthopedic surgery. It is designed for patients requiring hip joint replacement, typically used by orthopedic surgeons.
FDA Clearance Information
Pathway
510K
Number
K902436 ↗
Decision Date
August 29, 1990
Product Code
JDI
Device Class
Class 2
Evidence
0 studies
The HG Multilock Hip Prosthesis, manufactured by Zimmer, was cleared through the FDA 510k pathway on August 29, 1990. It is classified as a Class 2 device under product code JDI.
What It Is
The HG Multilock Hip Prosthesis is a medical device used in total hip arthroplasty. It features a Tinidium surface, which may enhance biocompatibility and reduce wear. The device is designed to replace the hip joint, providing stability and mobility for patients with hip joint degeneration or injury.
Clinical Applications
This prosthesis is commonly used in orthopedic surgeries for patients with osteoarthritis, rheumatoid arthritis, or traumatic hip injuries. It is typically employed in hospital settings by orthopedic surgeons. The device is suitable for adult patients experiencing severe hip pain and loss of function.
Indications for Use
The FDA indications suggest this device is intended for patients needing hip joint replacement due to conditions like arthritis or hip fractures. It is suitable for those who have not responded to conservative treatments.
Practical Considerations
The HG Multilock Hip Prosthesis comes in various sizes to accommodate different patient anatomies. It is important to ensure compatibility with other surgical instruments and components. Surgeons should be familiar with the implantation technique to optimize outcomes.
Frequently Asked Questions
What is the HG Multilock Hip Prosthesis used for?
It is used for hip joint replacement in patients with severe hip degeneration or injury.
What specialties typically use this device?
Orthopedic surgeons primarily use this device in total hip replacement surgeries.
What are the FDA-cleared indications?
The device is indicated for patients requiring hip replacement due to arthritis or hip fractures.
Disclaimer: This page compiles publicly available regulatory and published clinical evidence for educational reference.
It does not constitute medical advice, product endorsement, or a recommendation for clinical use.
Always consult manufacturer documentation and clinical judgment for patient care decisions.