The FDA has approved RSB Spine’s InterPlate C-Ti interbody fusion device for a new indication, as an anterior cervical plate, according to a release by RSB Spine.
When the FDA reclassified interbody fusion devices in 2007, the C-Ti was the first such device to be cleared and now it is the first interbody fusion device to be cleared as an anterior cervical plate.
Read RSB Spine’s release on FDA approval of its InterPlate C-Ti.
From findings on cervical disc replacement to total knee replacement, Becker’s reported on eight spine and orthopedic studies since March…
Researchers at UMass Chan Medical School in Worcester, Mass., have created an algorithm to predict total knee replacement outcomes in…
Orthopaedic Solutions Management has acquired Orlando Hand Surgical Associates, marking its eighth acquisition. OHSA was founded in 2000 and has…
Comments are closed.