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monospherical resurfacing glenoid pros
Howmedica
Summary: The monospherical resurfacing glenoid pros by Howmedica is a medical device used in shoulder arthroplasty. It is primarily utilized by orthopedic surgeons to address joint degeneration.
FDA Clearance Information
Pathway
510K
Number
K833409 ↗
Decision Date
November 7, 1983
Product Code
KWT
Device Class
Class 2
Evidence
0 studies
The device was cleared through the FDA's 510k pathway on November 7, 1983. Manufactured by Howmedica, it is classified as a Class 2 device under the product code KWT.
What It Is
The monospherical resurfacing glenoid pros is a prosthetic component designed for shoulder joint resurfacing. It is used in shoulder arthroplasty procedures to replace or resurface the glenoid, the socket part of the shoulder joint. This device helps restore joint function and alleviate pain in patients with degenerative joint conditions.
Clinical Applications
This device is commonly used in orthopedic surgery, specifically in shoulder arthroplasty procedures. It is suitable for patients with osteoarthritis, rheumatoid arthritis, or post-traumatic arthritis of the shoulder. The device is typically used in hospital settings by orthopedic surgeons specializing in joint replacement.
Indications for Use
The device is indicated for patients requiring shoulder joint resurfacing due to degenerative conditions. It is intended for those with significant joint pain and dysfunction that have not responded to conservative treatments.
Practical Considerations
The device comes in various sizes to accommodate different patient anatomies. It is important to ensure compatibility with other prosthetic components used in shoulder arthroplasty. Surgeons should be familiar with the specific surgical techniques required for implantation.
Frequently Asked Questions
What is monospherical resurfacing glenoid pros used for?
It is used for shoulder joint resurfacing in arthroplasty procedures to alleviate pain and restore function in patients with degenerative joint conditions.
What specialties typically use this device?
Orthopedic surgeons specializing in joint replacement and shoulder arthroplasty typically use this device.
What are the FDA-cleared indications?
It is indicated for patients with degenerative shoulder joint conditions requiring resurfacing, such as osteoarthritis or rheumatoid arthritis.
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.