TruSpine Technologies PLC Survey of Cervi-LOK(TM) (0346A)
May 27 2021 - 4:03AM
UK Regulatory
TIDMTSP
RNS Number : 0346A
TruSpine Technologies PLC
27 May 2021
TruSpine Technologies plc
("T ruSpine" or the "Company")
Survey of Cervi-LOK(TM)
TruSpine Technologies plc, (AQSE: TSP) the medical device
company focused on the development of its proprietary, pioneering
"screwless," spinal (vertebral) stabilisation system, announces
that its cornerstone Cervi-LOK(TM) device has completed Round II
testing.
Round II testing consisted of a cadaver study which was
conducted at the Upstate Medical School in Syracuse, New York, and
was performed by two highly experienced surgeons who are also
members of TruSpine's medical advisory board: Dr. Mark Smith /
Neurosurgeon (tested on May 6) and Dr. William Lavelle /
Orthopaedic spine surgeon (tested on May 7). Also in attendance was
Nathan Erickson, the Lead Engineer from TruSpine's engineering
partner, LincoTek, Inc., as well as Professor Frank Boehm,
TruSpine's Chief Technical Consultant.
The objectives of the cadaver study included evaluating the
usability of the instruments to implant the system, as well ease of
insertion, grasp of the vertebrae and strength of the implant
system. T he surgeons conducted their study independent of one
another, further enhancing the validity of the evaluation. The
procedures were recorded on video, and pending editing, this should
be available for general viewing on the TruSpine website in due
course.
A stabilisation from the C2 to C5 vertebrae was achieved, on
average in less than 15 minutes; in one instance, a unilateral
stabilisation was achieved in 14 minutes from the time of the
initial skin incision until the time of complete insertion of the
implant, which is an exceptional outcome relative to current
technologies as detailed below, even for a highly skilled
surgeon.
No X-Rays were required, no injury to the bone was noted, and -
as further confirmation of the benefits of the system, there was no
possibility of injury to vascular or neurologic structures. This is
in contrast to current technology, which can take 30 to 45 minutes
or longer, requires significant intraoperative X-Rays, and can be
complicated by injuries to critical blood vessels, nerves or even
the spinal cord.
Dr. Smith was particularly impressed with the versatility and
flexibility of the device and Dr. Lavelle thought that the system
was excellent, noting some additional indications beyond those
originally stated.
The overall view of both participating surgeons was that the
system was extremely effective, efficient and has a great deal of
appeal to practicing surgeons, with ease and convenience and
avoidance of injury to critical structures. In addition, the
Cervi-LOK (TM) system was highly praised for its flexibility and
versatility and it was mutually agreed that the potential for
commercial success was high.
Ian Roberts, CEO of TruSpine Technologies plc, commented: "We
are delighted to receive this compelling feedback on the
Cervi-LOK(TM) system by highly experienced surgeons. Both surgeons
involved are extensively trained in their field, and gave
invaluable insights into the product performance.
"We have concluded that Cervi-LOK(TM) offers other advantages
previously not considered, including as a rescue technique for
failed lateral mass screws, or as a topping off procedure for
deformity constructs. Both surgeons universally agreed that the
convenience and low risk nature of the system make it a very
attractive alternative to the current screw technologies. This
evidence is very advantageous to us as we progress towards FDA
application and clearances."
Enquiries:
Truspine Technologies Plc Tel: +44 (0)20 3638 5025
Ian Roberts, CEO
Cairn Financial Advisers LLP (AQSE Corporate Tel: +44 (0)20 7213
Adviser) 0880
Liam Murray / Ludovico Lazzaretti
WH Ireland (Broker) Tel: +44 ( 0)20 7220 1666
Adam Pollock
Walbrook PR (Financial PR Tel: +44 (0) 20 7933 7870 or +44
& IR) (0) 7876 741 001
Anna Dunphy truspine@walbrookpr.com
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