Aesculap knee implant systems used advanced surface technology which may have contributed to loosening of the device after knee replacement surgery.
Aesculap ceramic knee.
Aesculap s gold knee with its patented seven layer advanced surface technology offers enhanced protection against the top prostheses related reasons for implant failure and revision.
In combination with our beta sterilized gliding surface the system offers state of.
The lawsuit alleges a.
Instead of allowing moisture inside a patient s body the ceramic coating repels the moisture and causes the moisture to gather on the implant s surface under the bone cement which is supposed to attach to a patient s leg bone.
The ceramic coating used in aseculap knee.
Braun subsidiary aesculap implant systems knew about a problem with its line of ceramic coated artificial knees but failed to take.
More information on aesculap knee replacement complications.
The established advanced surface technology creates one of the hardest surfaces and enables allergy prevention.
Braun regarding a problem with the company s prosthetic knee replacement devices.
Zirconium itself is one of the most biocompatible metals available.
There have been an increasing number of adverse events reported to the fda since january 2016 regarding surgeons revising failed aesculap vega systems devices for aseptic loosening non infection related where the surgeon notes the complete absence of cement bonded to either the femoral or tibial components.
1 with approximately 20 of all tka patients reporting dissatisfaction with their knee replacements 2 now is the perfect time to learn more about our gold knee.
A lawsuit on behalf of 30 knee replacement patients alleges b.
Aesculap vega knee devices are ceramic coated implants created to eliminate the loss of metal ions within the body.
Like many modern day knee replacements on the market the aesculap system utilizes the advanced surface technology ceramic coating which was originally thought to be safer than the metal implants that have come under significant scrutiny.
According to the suit the company was aware of the problem with the effectiveness of the bonding agent used in its ceramic coated knee replacement devices but did not correct the problem or warn consumers of the risk.
The manufacturer of these devices b.
Many people who received these implants have filed aesculap knee replacement lawsuits due to implant failure and a need for revision surgery.
A new lawsuit was just filed against aesculap a division of b.
Univation x is an unicondylar knee arthroplasty system for treatment of medial osteoarthritis.
Material for durability the ceramic surface reduces polyethylene wear and increases scratch resistance.
Is there a recall for aesculap knee replacement systems.
As of early spring 2018 there has been no official recall issued for aesculap knee replacement devices.
