Tag: Invibio
“The best of all worlds”: A surgeon’s clinical experience with the...
This advertorial has been sponsored by INVIBIO ™
Hyun W Bae, MD, is a medical director at The Spine Institute (Saint John’s Health Center, Santa...
A neurosurgeon’s experience with PEEK-OPTIMA™ HA Enhanced devices
This advertorial has been sponsored by INVIBIO™
Jill Wright Donaldson, MD, is a neurosurgeon at Community Hospital North (Indianapolis, IN, USA), specialising in the surgical...
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...
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...
Rectifying a failed titanium fusion with PEEK-OPTIMA™ HA Enhanced cage and...
This case report is sponsored by INVIBIO™
To view this case report as a PDF, please click here.
Timothy Bassett, MD (SouthEastern Spine Specialists, Tuscaloosa, AL,...
Case report: Successful lumbar interbody fusion with PEEK-OPTIMA™ HA Enhanced cage...
Timothy Bassett, MD (SouthEastern Spine Specialists, Tuscaloosa, AL, USA) has over 23 years of experience in spinal surgery, predominantly in the treatment of adult...
Case Series: Early clinical results for cervical and lumbar fusion
Timothy Bassett, MD, of SouthEastern Spine Specialists and Brad Prybis, MD of Carrollton Orthopaedic Clinic share their early clinical experience with interbody fusion devices...
SeaSpine receives two US FDA 510(k) clearances
SeaSpine has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Shoreline ACS anterior cervical standalone system, featuring TruProfile technology,...