MEMPHIS, TENN. - Dec. 6, 2013 - Medtronic, Inc. (MDT) presented 7-year clinical and radiographic outcomes of artificial disc replacement with PRESTIGE® Cervical Disc compared to anterior cervical ...
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 ...
DUBLIN and CHICAGO - October 15, 2015 - Medtronic plc (MDT) today announced favorable seven-year data maintaining improved clinical outcomes and patient satisfaction for the Prestige LP(TM) Cervical ...
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 ...
We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio CHICAGO — Segmental motion in the ...
Reoperation rates between cervical disc replacement and anterior cervical discectomy and fusion didn’t see significant differences in reoperation risks. However disc replacement had some advantage in ...
Ten-year follow-up data indicates discs next to fusion required surgery twice as often as discs next to artificial discs. The most compelling data from the 10-year follow-up is that the discs next to ...
Usually the first step is conservative treatment. Patients who have radicular symptoms but who do not have weakness or myelopathy can be treated conservatively. Conservative treatment can include ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results