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glenoid resurface component pmn 3m
3M
Summary: The Glenoid Resurface Component PMN 3M is a medical device used in orthopedic surgeries to address joint surface damage. It is primarily used by orthopedic surgeons in procedures involving the shoulder joint.
FDA Clearance Information
Pathway
510K
Number
K831234 ↗
Decision Date
June 2, 1983
Product Code
KWT
Device Class
Class 2
Evidence
0 studies
The Glenoid Resurface Component PMN 3M was cleared through the FDA 510(k) pathway on June 2, 1983. It is manufactured by 3M and classified as a Class 2 device under product code KWT.
What It Is
The Glenoid Resurface Component PMN 3M is designed to replace or resurface the glenoid cavity of the shoulder joint. It is typically made of biocompatible materials that mimic the natural joint surface, helping to restore function and reduce pain in patients with joint degeneration or damage. This device is crucial in maintaining joint stability and mobility, particularly in patients with arthritis or traumatic injuries.
Clinical Applications
This device is commonly used in orthopedic surgeries, particularly in shoulder arthroplasty procedures. It is suitable for patients with osteoarthritis, rheumatoid arthritis, or those who have suffered traumatic injuries to the shoulder. Orthopedic surgeons in hospital settings or specialized orthopedic centers typically use this device to improve joint function and patient quality of life.
Indications for Use
The Glenoid Resurface Component PMN 3M is indicated for patients who require joint surface replacement due to conditions like arthritis or trauma. It is specifically used to address damage to the shoulder joint, helping to alleviate pain and restore mobility.
Practical Considerations
The device comes in various sizes to accommodate different patient anatomies and is compatible with other standard shoulder arthroplasty components. Surgeons should consider the patient's specific joint anatomy and the extent of joint damage when selecting the appropriate size and type of component.
Frequently Asked Questions
What is the Glenoid Resurface Component PMN 3M used for?
It is used to replace or resurface the glenoid cavity of the shoulder joint in patients with joint damage.
What specialties typically use this device?
Orthopedic surgeons specializing in shoulder surgeries typically use this device.
What are the FDA-cleared indications?
It is indicated for joint surface replacement in patients with shoulder joint damage due to arthritis or trauma.
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.