đź“‹ FDA Reference
arthrosurface kissloc knotless suture system
Arthrosurface
Summary: The Arthrosurface KISSloc Knotless Suture System is a medical device used for soft tissue fixation in orthopedic surgeries. It is primarily used by orthopedic surgeons to repair meniscal tears and other soft tissue injuries.
FDA Clearance Information
Pathway
510K
Number
K133835 ↗
Decision Date
July 3, 2014
Product Code
HTN
Device Class
Class 2
Evidence
0 studies
The Arthrosurface KISSloc Knotless Suture System was cleared through the FDA 510k pathway on July 3, 2014. It is manufactured by Arthrosurface and classified as a Class 2 device under product code HTN.
What It Is
The Arthrosurface KISSloc Knotless Suture System is designed for soft tissue fixation without the need for tying knots. It uses an anchor-based mechanism that allows for adjustable tensioning of the suture, providing secure fixation. This system is particularly useful in orthopedic procedures where precise and reliable tissue repair is necessary.
Clinical Applications
This device is commonly used in orthopedic surgeries, particularly for repairing meniscal tears in the knee. It is suitable for use in sports medicine and orthopedic settings, where surgeons require efficient and reliable methods for soft tissue fixation. The system is beneficial for patients with injuries requiring minimally invasive repair techniques.
Indications for Use
The FDA-cleared indications for the Arthrosurface KISSloc Knotless Suture System include its use in soft tissue fixation procedures. It is particularly indicated for patients with meniscal tears or other soft tissue injuries that require secure and adjustable fixation.
Practical Considerations
The system is designed to be compatible with standard arthroscopic instruments and techniques. It offers adjustable tensioning, which can be advantageous in achieving optimal tissue repair. Surgeons should be familiar with anchor-based fixation techniques to effectively use this device.
Related Literature
The linked study compared transtibial pull-out fixation with suture anchor fixation for medial meniscus posterior root tears. It found that the knotless adjustable suture anchor fixation demonstrated less cyclic displacement than the traditional pull-out repair. However, the study did not fully explore how meniscal extrusion and contact mechanics compare under cyclic tibiofemoral loading, indicating a need for further research.
Frequently Asked Questions
What is the Arthrosurface KISSloc Knotless Suture System used for?
It is used for soft tissue fixation in orthopedic surgeries, particularly for repairing meniscal tears.
What specialties typically use this device?
Orthopedic surgeons and sports medicine specialists commonly use this device.
What are the FDA-cleared indications?
The device is indicated for soft tissue fixation, especially in procedures involving meniscal tears and similar injuries.
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.