FDA Authorizes Marketing of MISHA™ Knee System for People Suffering from Knee Osteoarthritis
Moximed , a medical device company on a mission to improve the standard of care for people with knee osteoarthritis (OA), today announced that the U.S. Food and Drug Administration (FDA) granted marketing authorization of the MISHA™ Knee System, an implantable shock absorber (ISA) for the knee.
- Moximed , a medical device company on a mission to improve the standard of care for people with knee osteoarthritis (OA), today announced that the U.S. Food and Drug Administration (FDA) granted marketing authorization of the MISHA™ Knee System, an implantable shock absorber (ISA) for the knee.
- View the full release here: https://www.businesswire.com/news/home/20230410005434/en/
“I've been lucky enough to have been exposed to many major orthopedic innovations, most notably total knee arthroplasty (TKA). - For these patients, total knee replacement is a reluctant option, as it is an end-stage treatment for end-stage disease.
- OA patients without end-stage disease seek options that preserve their knee, activity level, and quality of life.