Orthofix Medical Inc., a global medical device company with a spine and orthopedics focus, announces U.S. FDA premarket approval for the AccelStim bone healing therapy Class III device. The AccelStim device provides a nonsurgical treatment for indicated fresh fractures and for fractures that have not healed (nonunions).
The device generates a low-intensity pulsed ultrasound (LIPUS) signal to stimulate the bone’s natural healing process to promote fracture healing. Commercial availability of the AccelStim device is anticipated to occur in the second quarter of this year through a targeted and phased launch plan.
“As the market leader in bone growth stimulation devices, more than a million patients have been treated with our pulsed electromagnetic field stimulation (PEMF) systems,” says Orthofix President of Global Spine Kevin Kenny. “With the addition of the AccelStim device, Orthofix is now the first and only company to offer both PEMF and LIPUS bone growth stimulation devices, and one of only two companies in the U.S. with a fresh fracture indication.”
Kenny adds, “We believe that expanding access to patients should help grow the existing $100 million market for fresh fracture LIPUS solutions. This investment and approval further demonstrates our leadership in and commitment to the bone growth stimulation market.”
The AccelStim device is worn externally in the region of the fracture, typically for 20 minutes daily. Treatment length may vary and is determined by the prescribing physician on an individual basis according to the fracture healing progress. The device is lightweight, adjustable, and portable, and includes a rechargeable battery that allows freedom of movement during treatment.
Morever, the AccelStim system includes a treatment calendar to engage patients in their recovery. The LIPUS technology stimulates bone healing at the molecular, cellular, and tissue level and has been proven to accelerate fracture-healing recovery by 38% for indicated fresh fractures and an overall clinical success rate of 86% for nonunion fractures. The AccelStim device provides a nonsurgical treatment for indicated fresh fractures and for fractures that have not healed (nonunions).
The device generates a low-intensity pulsed ultrasound (LIPUS) signal to stimulate the bone’s natural healing process to promote fracture healing. Commercial availability of the AccelStim device is anticipated to occur in the second quarter of this year through a targeted and phased launch plan.
“As the market leader in bone growth stimulation devices, more than a million patients have been treated with our pulsed electromagnetic field stimulation (PEMF) systems,” says Orthofix President of Global Spine Kevin Kenny. “With the addition of the AccelStim device, Orthofix is now the first and only company to offer both PEMF and LIPUS bone growth stimulation devices, and one of only two companies in the U.S. with a fresh fracture indication.”
Kenny adds, “We believe that expanding access to patients should help grow the existing $100 million market for fresh fracture LIPUS solutions. This investment and approval further demonstrates our leadership in and commitment to the bone growth stimulation market.”
The AccelStim device is worn externally in the region of the fracture, typically for 20 minutes daily. Treatment length may vary and is determined by the prescribing physician on an individual basis according to the fracture healing progress. The device is lightweight, adjustable, and portable, and includes a rechargeable battery that allows freedom of movement during treatment.
Morever, the AccelStim system includes a treatment calendar to engage patients in their recovery. The LIPUS technology stimulates bone healing at the molecular, cellular, and tissue level and has been proven to accelerate fracture-healing recovery by 38% for indicated fresh fractures and an overall clinical success rate of 86% for nonunion fractures.
