Hanger Orthopedic Group Receives 510(k) Clearance

BETHESDA, Md., Feb. 2 /PRNewswire-FirstCall/ -- Hanger Orthopedic Group,
Inc. (NYSE: HGR) has announced its wholly-owned subsidiary Innovative
Neurotronics, Inc. (IN, Inc.) received 510(k) clearance from the U.S. Food and
Drug Administration (FDA) to treat patients with the WalkAide System(R).
The first of IN, Inc.'s line of functional electrical stimulation
products, the WalkAide System is a medical device designed to counter the lack
of ankle dorsiflexion, commonly referred to as foot drop, in patients who have
sustained damage to upper motor neurons or pathways to the spinal cord. The
WalkAide System electrically stimulates the appropriate nerves and muscles.
In addition to improving the patient's gait, medical benefits of the WalkAide
System may include increased mobility, prevention/retardation of disuse
atrophy, increased local blood flow, muscle re-education, and maintained or
increased joint range of motion.
"The commercial introduction of the WalkAide System will help us achieve
our vision of providing high technology products in the neuromuscular field by
leveraging Hanger's assets in distribution and patient care centers," Chairman
of the Board and Chief Executive Officer of Hanger Orthopedic Group, Inc. Ivan
R. Sabel, CPO said.
Hanger also announced today IN, Inc.'s newly-appointed management team,
led by President Jeff Martin.
"IN, Inc. has taken a significant step forward in its evolution by
receiving FDA approval and creating a management team with the talent and
depth of experience to advance our mission and expand the field of Myo-
Orthotics Technology(R)," Martin said.

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