Tag: hydroxyapatite
SpineFrontier receives FDA approval for A-CIFT SoloFuse HA standalone system
The A-CIFT SoloFuse HA (SpineFrontier) has received FDA approval.
The company states that the A-CIFT SoloFuse HA standalone system was produced “to leverage the familiarity...
FDA 510(k) clearance for cervical and lumbar HA PEEK interbody...
The US Food and Drug Administration (FDA) has granted 510(k) clearance for both the ALTA ACDF interbody spacers (Astura Medical) and HALF DOME lumbar...
Omnia Medical gains FDA clearance for vertebral body replacement system
Omnia Medical has announced that the US Food and Drug Administration (FDA) has cleared its new vertebral body replacement (VBR) system, which is manufactured...
“Significantly more bone infiltration” with 3D-printed triangular sacroiliac joint fusion implants
The popularity of sacroiliac joint fusion has grown rapidly over the past five years, with SI-Bone’s Ifuse device leading the market. Recently approved by...
US FDA clears Spinal Simplicity Minuteman G3 hydroxyapatite-coated fusion device
Spinal Simplicity has launched a new generation of Minuteman G3 fusion device, featuring a US Food and Drug Administration (FDA)-cleared coating of hydroxyapatite.
"Hydroxyapatite has...