Orthofix Receives 510(k) Clearance and CE Mark for TrueLok Elevate Transverse Bone Transport System
19 Março 2025 - 9:00AM
Business Wire
Orthofix Medical Inc. (NASDAQ:OFIX), a leading global medical
technology company, today announced it has received U.S. Food and
Drug Administration (FDA) 510(k) clearance and the European CE Mark
for the TrueLok™ Elevate Transverse Bone Transport (TBT)
System.
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TrueLok™ Elevate Transverse Bone
Transport (TBT) System
TrueLok Elevate provides a limb preservation treatment option
for addressing bony or soft tissue deformities and defects such as
diabetic foot ulcers and nonhealing or deep tissue wounds. While
the TBT procedure has previously been reported,1 TrueLok Elevate is
the first dedicated system for TBT to receive FDA clearance. The
product is currently available in a limited market release in the
U.S. and select international markets.
“Transverse bone transport with TrueLok Elevate now enables
surgeons to effectively address challenging conditions in a
patient’s extremity by allowing for an efficient and reproducible
method to create a bone segment in the tibia that can then be
gradually distracted over a period of several days,” said Dr. Emmy
Oji, a podiatric foot and ankle surgeon at Valley Foot and Ankle
Specialty Providers, who was among the first surgeons to apply the
TrueLok Elevate system to a patient. “Clinical publications have
shown this approach improves blood circulation to the affected limb
and promotes wound healing in diabetic foot, potentially reducing
the need for amputation.” Additionally, first patient cases in
Europe were performed in the UK and Germany.
According to the American Diabetes Association, over 160,000
amputations occur per year in the U.S. as a result of
diabetic-related complications, representing a sizable market
opportunity of approximately $1.2 billion. In addition, published
studies have shown that patients with diabetic foot ulcers who
receive an amputation have a five-year mortality rate of 57% and
are burdened with lifetime healthcare costs of just over $640,000
for care directly related to their amputation.2,3 Therefore,
TrueLok Elevate offers the potential to not only be a limb and
cost-saving device, but most importantly, a life-saving solution to
a challenging patient population.
“The introduction of the TrueLok Elevate system is a pivotal
milestone in demonstrating our commitment to leading growth in the
limb reconstruction market,” said Patrick Fisher, President of
Global Orthopedics for Orthofix. “Within our orthopedics business,
we are focusing on providing innovative solutions that spans four
pillars: Limb Preservation, Extremity Deformity Correction, Limb
Lengthening, and Complex Fracture Management to aid surgeons in
managing patients with complex limb reconstruction needs.”
Those attending the American College of Foot & Ankle
Surgeons (ACFAS) Annual Scientific Conference in Phoenix, AZ from
March 27-30 can learn more about the TrueLok Elevate System by
visiting booth 1045.
The TrueLok Elevate system represents the latest addition to
Orthofix’s flagship product line, the TrueLok family of multiplanar
external fixators, including the TrueLok EVO and TL-HEX™ ring
fixation systems. For indications, contraindications, warnings,
precautions, potential adverse effects, and patient counseling
information see the Instructions for Use or contact your local
representative. Additional information about Orthofix’s full line
of orthopedic solutions is available on Orthofix.com.
References:
1. Chen, Yan et al. “Effect of tibial cortex transverse
transport in patients with recalcitrant diabetic foot ulcers: A
prospective multicenter cohort study.” Journal of orthopaedic
translation vol. 36 194-204. 12 Oct. 2022,
doi:10.1016/j.jot.2022.09.002
2. Vuorlaakso, Miska et al. “Major Amputation Profoundly
Increases Mortality in Patients With Diabetic Foot Infection.”
Frontiers in surgery vol. 8 655902. 30 Apr. 2021,
doi:10.3389/fsurg.2021.655902
3. Palli, S et al. “Impact of a limb salvage program on the
economic burden of amputation in the United States.” Value in
health vol. 19 Issue 3, A45
About Orthofix
Orthofix is a global medical technology company headquartered in
Lewisville, Texas. By providing medical technologies that heal
musculoskeletal pathologies, we deliver exceptional experiences and
life-changing solutions to patients around the world. Orthofix
offers a comprehensive portfolio of spinal hardware, bone growth
therapies, specialized orthopedic solutions, biologics and enabling
technologies, including the 7D FLASH™ Navigation System. To learn
more, visit Orthofix.com and follow Orthofix on LinkedIn.
Forward-Looking Statements
This news release may include forward-looking statements within
the meaning of Section 21E of the Securities Exchange Act of 1934,
as amended, and Section 27A of the Securities Act of 1933, as
amended. In some cases, you can identify forward-looking statements
by terminology such as “may,” “will,” “should,” “expects,” “plans,”
“anticipates,” “believes,” “estimates,” “projects,” “intends,”
“predicts,” “potential,” “continue” or other comparable
terminology. Orthofix cautions you that statements included in this
news release that are not a description of historical facts are
forward-looking statements that are based on the Company’s current
expectations and assumptions. Each forward-looking statement
contained in this news release is subject to risks and
uncertainties that could cause actual results to differ materially
from those expressed or implied by such statement. Applicable risks
and uncertainties include, among others: the ability of newly
launched products to perform as designed and intended and to meet
the needs of surgeons and patients, including as a result of the
lack of robust clinical validation; and the risks identified under
the heading “Risk Factors” in Orthofix Medical Inc.’s Annual Report
on Form 10-K for the fiscal year ended December 31, 2024, which was
filed with the Securities and Exchange Commission (SEC) on February
25, 2025, as well as any subsequent Quarterly Report on Form 10-Q
or Current Report on Form 8-K filed with the SEC. The Company’s
public filings with the SEC are available at www.sec.gov. You are
cautioned not to place undue reliance on forward-looking
statements, which speak only as of the date when made. Orthofix
does not intend to revise or update any forward-looking statement
set forth in this news release to reflect events or circumstances
arising after the date hereof, except as may be required by
law.
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Investors and Media Julie Dewey, IRC Chief Investor
Relations & Communications Officer JulieDewey@orthofix.com
209.613.6945
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