If you are a medical device manufacturer dealing with the lack of options for young knee patients — this project developed the Trammpolin prosthesis that restores mobility and postpones total knee replacement. It uses a minimally invasive arthroscopic approach to fill a treatment gap affecting 350,000 patients.
Advanced Lateral Meniscus Prosthesis to Prevent Knee Replacement in Younger Patients
Imagine your knee has a built-in shock absorber called the meniscus. When this part wears out or is removed, the knee joint grinds down, causing severe pain. This project creates a high-tech replacement part made of special plastics that mimics the natural cushion, acting like a new shock breaker for the leg.
What needed solving
Young patients with lateral meniscus damage face a 13-year treatment gap where they must rely on painkillers until they are old enough for a total knee replacement. This results in massive healthcare costs and lost productivity.
What was built
A lateral meniscus prosthesis called Trammpolin made of two biocompatible polymers, including a fixation method using ligament tape.
Who needs this
Who can put this to work
If you are a clinic dealing with high patient demand for knee osteoarthritis treatments — this project developed a flexible implant that reduces peak pressure on cartilage. This allows you to offer a solution to the 70,000 new lateral patients entering the pool every year.
If you are an insurer dealing with the economic burden of lateral KOA costing €40K-€79k per patient — this project developed a durable prosthesis that reduces medication dependency and absenteeism. This lowers the long-term healthcare costs associated with chronic knee disability.
Quick answers
What is the estimated cost or economic impact per patient?
The economic burden of lateral knee osteoarthritis is estimated between €40K and €79k per patient due to medical costs, absenteeism, and disability.
Is the technology ready for industrial scale production?
The project is currently optimizing design and conducting a First In Human-study to achieve CE-marking for a planned market entry in 2026.
What is the IP status or licensing potential?
Based on available project data, the technology has already received the Breakthrough Device Designation from the US FDA in 2020 for the medial version.
What regulatory hurdles remain?
The project must obtain CE-marking and perform a health economics analysis to secure reimbursement from medical systems.
What is the timeline for commercial availability?
The target for successful market entry is 2026.
Who built it
The project is led by a single SME, ATRO Medical BV from the Netherlands. This 100% industry-led structure indicates a strong commercial drive and a streamlined decision-making process, focusing on rapid transition from lab testing to CE-marking and market entry.
Contact ATRO Medical BV in the Netherlands regarding the Trammpolin lateral prosthesis.
Talk to the team behind this work.
Contact us to explore licensing opportunities for biocompatible polymer implants.