www.fdanews.com/articles/187472-arthrosurface-cleared-to-market-patellofemoral-arthroplasty-system
Arthrosurface Cleared to Market Patellofemoral Arthroplasty System
July 4, 2018
The FDA granted 510(k) clearance for Arthrosurface’s patellofemoral WaveKahuna arthroplasty system, an extension of the company’s Hemicap Patellofemoral & PF Wave Systems product family.
The WaveKahuna system is designed to restore the patella and femoral trochlea’s surface geometry and preserve the patient’s knee.
The system introduces larger implants, which gives surgeons a wider variety of size offerings for patients.