Synergy Spine Solutions has received premarket approval (PMA) from the US Food and Drug Administration (FDA) for the Synergy ...
Synergy Spine Solutions announced today that it received FDA premarket approval (PMA) for its Synergy Disc for 1-level ...
The FDA recently approved the Medtronic Prestige LP Cervical System for treating degenerative disc disease at two adjacent vertebral levels (between C3 and C7). The device is said to be Medtronic’s ...
LOS ANGELES, Oct. 23, 2019 /PRNewswire-PRWeb/ -- In a new study, authored by Dr. Todd H. Lanman and Matthew F. Gornet, MD, and published in the prominent peer-reviewed medical journal Journal of ...
TA Criterion 1: The technology must have final approval from the appropriate government regulatory bodies. The Prestige® Cervical Disc (Medtronic Sofamor Danek, Memphis, TN) received FDA Premarket ...
Synergy Spine Solutions earned the FDA’s premarket approval for its Synergy Disc, according to a Feb. 27 news release. The device is approved for 1-level cervical disc replacement at C3 to C7 for ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Early composite clinical success showed similar outcomes ...
AxioMed Opens $10 Million Second Round to Fund Multi-Level Cervical IDE and Expand Commercialization
MALDEN, Mass.--(BUSINESS WIRE)--AxioMed closed an oversubscribed first round of funding from surgeons and high net worth individuals. Its second round for $10 million currently has pledges prior to ...
Please provide your email address to receive an email when new articles are posted on . Medtronic announced it has received FDA approval of the Prestige LP cervical disc for treatment of cervical disc ...
LEWISVILLE, Texas--(BUSINESS WIRE)--Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and orthopedics focus, today announced the first patient implant in a U.S. Food ...
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