The FDA has cleared home use of a device that helps people with spinal cord injuries regain mobility and functioning.
Onward’s Arc-Ex earned FDA 510(k) clearance for use at home, according to a Nov. 17 news release. The device is cleared for “use in conjunction with functional task practice in the clinic and ...
University Orthopedics’ East Bay Surgery Center in East Providence, R.I., has become the first site in the state to implant a closed-loop spinal cord stimulator. Shiqiang “Chris” Tian, MD, an ...
Onward Medical announced today that it received FDA 510(k) clearance to expand the ARC-EX system's indication for home use.
Centennial Spine and Pain joined us at the New Mexico Living studio on Monday for our weekly health segment. This week, Dr.
Medical Device Network on MSN
FDA clears Onward’s ARC-EX System for home use in spinal cord injury care
The US Food and Drug Administration (FDA) has granted 510 (k) clearance for the expanded use of Onward Medical’s ARC-EX ...
Zacks Investment Research on MSN
BSX's Neuromodulation Prospect Looks Strong: What's Behind It?
The rising incidences of chronic pain, neurological disorders and mental health conditions continue to drive the demand for global neuromodulation devices. According to Grand View Research, the market ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback