Artelon CMC Spacer Lawsuit


The plaintiff filed this Artelon CMC Spacer lawsuit after he suffered permanent injuries after using the device. Plaintiff suffered from increased pain and reduced hand function, as well as permanent impairment of his CMC joint. As the defendants should have known about Spacer’s defective design, they failed to warn the plaintiffs of these risks. The First Amended Complaint asserts a defective design, inadequate warning, and liability for failure to conform to representations. The Fourth Amended Complaint alleges alternative liability on the part of the company as a supplier.

Artelon CMC Spacer

If you have been injured by a defective medical device, you may be able to receive financial compensation through an Artelon CMC Spacer lawsuit. The implant was meant to replace the cushion in the hand of patients with osteoarthritis. Manufacturers marketed the device as providing stability, pain-free recovery, and quick recovery. Unfortunately, the device has been linked to numerous FDA complaints and failures. As such, it’s important to contact an injury attorney to protect your rights and seek the compensation you deserve.

The Artelon CMC spacer is an implant that was approved by the FDA in 2007 and is used to treat early and mid-stage osteoarthritis of the carpometacarpal thumb joint. Patients reported problems including inflammation, pain, and reduced mobility. Some suffered severe deterioration of bone and required revision surgery. These complications have led to injuries, pain, and increased disability. If you’re one of the many people who suffered from pain and disability after receiving the Artelon CMC Spacer, you’re not alone. This implant has a dangerous side effect and may not be safe for you.

Aside from these problems, the Artelon CMC Spacer may also have caused the injury. It is designed to reduce pain and keep the thumb strong, but this has resulted in significant complication rates for patients. For these reasons, a class action lawsuit has been filed against the device manufacturer. Small Bone Innovations, Inc. has agreed to settle a lawsuit that is aimed at restoring the lives of patients suffering from this condition.

Artelon SST Spacer

If you are a person who has suffered from a serious injury due to a defective medical device, you may be eligible for a settlement from the manufacturer of the Artelon SST Spacer. The spacer is implanted inside the Scaphotrapezium-Trapezoid Joint. It was found that patients who have undergone this product have experienced several problems before and after the procedure. These issues have led many people to undergo additional surgeries to remove the product. These surgeries involved the borrowing of tendons from other parts of the body.

The device was approved for use in the treatment of patients with carpometacarpal joint arthritis. It is marketed as a safe, effective device that will provide relief from pain and improve range of motion. Despite the widespread complaints, the device has failed at a high rate. Because of these problems, attorneys urge those who have suffered from the Artelon SST Spacer to seek counsel immediately. An injury attorney in Florida will fight to ensure that you receive maximum financial compensation for your pain and suffering.

This lawsuit was filed by a person who suffered from a debilitating disorder caused by a defective medical device. The device was approved by the FDA in 2007 through the streamlined 510(K) process instead of the traditional Pre-Marketing Approval (PMA) process. The spacer was designed to provide relief from pain and reduce joint instability in people with osteoarthritis of the hand and thumb. The device was designed to provide patients with minimal pain and quick recovery. It was approved for use in patients with carpometacarpal joint osteoarthritis.

Artelon T-shaped spacer

The medical device industry is faced with a lawsuit over the safety of the Artelon CMC spacer, a T-shaped joint implant. The device was introduced in 2007 and was cleared by the FDA through the expedited 510(K) process, without a traditional Pre-Marketing Approval (PMA) process. It was designed to replace a missing bone between the first metacarpal bone and trapezial bone to treat osteoarthritic conditions in the thumb. The device promises stability, pain reduction, and a quick recovery.

However, many patients have experienced complications with the implant, and this has led to painful revision surgeries. Some patients have reported that their implants have fractured inside the hand, causing pain and swelling. Another patient, Kon, had surgery to remove the implant. After suffering through months of agonizing pain, she searched the web for other patients who had suffered similar experiences. Artimplant faces a lawsuit due to an unsafe medical device, and Kon has filed a personal injury lawsuit against the company.

The Artelon T-shaped spacer is made of biodegradable polycaprolactone fibers and is intended for use in people with early to midstage osteoarthritic of the thumb. The implant is inserted through a small dorsal radial thumb incision, which is used to expose the bone. In addition, the implant facilitates the ingrowth of healthy bone underneath it.

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