FDA Approves ViMove for Expanded Use in the United States
June 01 2015 - 3:05AM
Business Wire
Medical device company dorsaVi Ltd (ASX:DVL) has received 510(k)
clearance by the US Food and Drug Administration expanding the use
of ViMove in the United States.
The expanded functionality and labelling is highly significant
because for the first time in the USA it permits the use of ViMove
to display lower back and pelvic range of motion from healthy
patients (normative data). Clinicians and their patients will now
be able to compare how their movements are tracking against a
“normal” population based on their age group, and help guide
therapy decisions and rehabilitation accordingly.
Importantly, this new expanded labelling also permits dorsaVi to
record, assess and report on additional static postures including
lumbar lordosis (natural standing posture) and on various sitting
postures. The inclusion of the pelvic movement data allows
clinicians to independently isolate lumbar spine and pelvic
movements.
As part of the submission to achieve the new labelling, the
ViMove data was validated against sophisticated optical tracking
sensors (Vicon) used in biomechanical laboratories, and with a
marker set clinically validated against Magnetic Resonance Imaging
(MRI) for a range of lumbopelvic movements. All ViMove data for
standing and sitting postures was accurate to within 5 degrees.
“This is an important breakthrough for clinicians and patients,”
said Andrew Ronchi, CEO of dorsaVi.
ViMove was previously 510(k) cleared in July 2014 and with this
latest clearance, improves the clinical capabilities of ViMove.
John Kowalczyk, President of dorsaVi USA added: “510(k)
clearance by the FDA, which enables the expanded use of ViMove in
the United States, is a major milestone for dorsaVi and will allow
us to increase our marketing efforts to physical therapists and
health care professionals globally.”
About dorsaVi
dorsaVi Ltd (ASX: DVL) is an ASX company focused on developing
innovative motion analysis device technologies for use in clinical
practice, elite sports, and occupational health and safety. dorsaVi
believes its wearable sensor technology enables – for the first
time – many aspects of detailed human movement and position to be
accurately captured, quantified and analysed outside a biomechanics
lab, in both real-time and real situations for up to 24 hours.
Our technology has application across three sectors:
- Clinical: ViMove is transforming
the management of patients, by providing objective assessment,
monitoring outside the clinic and tailored biofeedback. ViMove is
currently used by medical and allied health practice in Australia,
New Zealand and the United Kingdom.
- Elite Sports: Elite sports
medical teams are using ViPerform to screen and assess risk of
injury, take preventative action, optimize technique, improve
athlete rehabilitation, and make better return to competition
decisions. ViPerform is being used by AFL and NRL clubs in
Australia, clubs in the Barclays Premier League, Australian and
Victorian Institutes of Sport, Cricket Australia and various
Olympic teams and athletes internationally.
- OHS: We combine innovation,
measurement and quality to reduce workplace incidents, costs, meet
compliance and improve brand reputation. ViSafe enables employers
to assess risk of injury for employees as well as test the
effectiveness of proposed changes to workplace design, equipment or
methods based on objective evidence. ViSafe has been used by major
corporations including Coles, Woolworths, Toll, Toyota, Orora
(formerly Amcor), Crown and BHP Billiton. Australian Workplace
Compliance (AWC) delivers risk mitigation through compliance to
OHS, Quality Management Systems, Company Policy and Process.
Further information is available at www.dorsavi.com.
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For more information or to arrange an interview, please
contact:Kellie Hanrick (Media)Buchan
Consultingkhanrick@buchanwe.com.au0413 681 346orRebecca Wilson
(Investor Relations)CEO, Buchan
Consultingrwilson@buchanwe.com.au(03) 9866 4722 / 0417 382 391
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