Tag: ALIF
Astura Medical receives FDA 510(k) clearance for El Capitan X expandable...
Astura Medical has announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA) for its El Capitan X expandable...
ChoiceSpine announces line extension of their Harrier standalone ALIF system
ChoiceSpine has announced the launch of an additional 20° lordotic offering for their standalone anterior lumbar interbody—Harrier SA. Harrier SA is a 3D-printed standalone...
CTL Amedica gains FDA clearance for MONDRIAN ALIF cage system with...
CTL Amedica has received official 510(k) clearance from the US Food and Drug Administration (FDA) to market its MONDRIAN anterior lumbar interbody fusion (ALIF)...
Stryker launches Monterey AL interbody system
Stryker has announced the launch of the Monterey AL interbody system, a standalone interbody fusion device designed for anterior lumbar interbody fusion (ALIF).
Monterey AL...
Life Spine announces FDA 510(k) clearance for its GHOST 3D-printed titanium...
Life Spine has received clearance from the US Food and Drug Administration (FDA) to market the GHOST 3D-printed titanium spacer system, which includes new...
SeaSpine announces full commercial launch of Meridian anterior lumbar interbody system
SeaSpine has announced the full commercial launch of its Meridian anterior lumbar interbody fusion (ALIF) system featuring the Reef A interbody.
The Meridian anterior lumbar...
Nexus Spine announces beta launch of Stable-C cervical interbody system with...
Nexus Spine has announced the beta launch of its Stable-C cervical interbody fusion implants featuring integrated anchoring blades.
The limited release adds to the company’s growing...
Theradaptive secures breakthrough device designation for spinal fusion implant
Theradaptive has announced that the US Food and Drug Administration (FDA) has granted breakthrough medical device designation for the use of its OsteoAdapt SP...
Aurora Spine receives FDA 510(k) clearance for its DEXA SOLO-L ALIF...
Aurora Spine has announced that it has received US Food and Drug Administration (FDA) 510(k) clearance for its 3D-printed DEXA SOLO-L anterior lumbar interbody...
ChoiceSpine launches Harrier standalone anterior lumbar interbody fusion system
ChoiceSpine has announced the full market release of its next-generation Harrier standalone anterior lumbar interbody fusion (ALIF) system.
Harrier SA is a 3D-printed standalone screw-based...
Astura Medical bags FDA 510(k) clearance for El Capitan Oblique ALIF...
Astura Medical has announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA) for its El Capitan Oblique anterior...
Underweight patients at greater risk of postoperative adverse events following stand-alone...
Patients who are underweight are more likely to experience postoperative adverse events following stand-alone anterior lumbar interbody fusion (ALIF) than those who have either...
Hedron IA 3D printed ALIF spacer used in vertebral body fixation...
Globus Medical has announced the first procedure using the Hedron IA implant, a 3D printed integrated ALIF spacer that leverages anchors or screws for...
NuVasive launches Brigade Lateral implant and instrumentation optimised for lateral ALIF...
NuVasive has announced the US commercial launch of Brigade Lateral, the industry's first interbody implant and instrumentation optimised for lateral anterior lumbar interbody fusion...
Renovis Surgical receives FDA clearance for Tesera Trabecular Technology Hyperlordotic ALIF...
Renovis Surgical Technologies has announced that it has received 510(k) clearance from the US Food and Drug Administration (FDA) to market the Tesera SA...
Fortilink-TS and –L IBF systems with TETRAfuse 3D technology launches commercially
The commercial launch of Fortilink-TS and –L IBF systems (RTI Surgical) with TETRAfuse 3D technology has added to a growing series of interbody fusion...
Rampart One standard ALIF interbody fusion system gains FDA clearance for...
The Rampart One Standard anterior lumbar interbody fusion (ALIF) device (Spineology) has been granted FDA clearance, allowing it to be used with or without...
Camber Spine announces 510(k) approval of ENZA-A titanium ALIF
The US Food and Drug Administration (FDA) has given 510(k) clearance to Camber Spine to market its ENZA-A titanium anterior lumbar interbody fusion (ALIF)...
FDA approval for Infuse Bone Graft in expanded spinal surgery indications
Infuse Bone Graft (Medtronic) has gained US Food and Drug Administration (FDA) approval in new spine surgery indications. InfuseBone Graft is now approved for...
Disability scores improve for all patients undergoing surgery with a Luna...
Positive interim results of a retrospective analysis of the Luna 3D multi-expandable interbody fusion system were announced by Benvenue Medical at the Annual Meeting...
Rigid, low-profile design ALIF system receives alpha release
Life Spine have announced that their Sentry plating system, which has been designed to improve lumbar stabilisation in anterior lumbar interbody fusion (ALIF) procedures,...
2 Rigid, low-profile design ALIF system receives alpha release
Life Spine have announced that their Sentry plating system, which has been designed to improve lumbar stabilisation in anterior lumbar interbody fusion (ALIF) procedures,...
Camber Spine launches Spira open matrix ALIF device
Camber Spine Technologies has launched its Open Matrix ALIF device in the USA following the receipt of 510(k) clearance from the US Food and...
Camber Spine exceeds 150th Enza ALIF implantation
Camber Spine Technologies has exceeded 150 implantations of the Enza zero-profile anterior lumbar interbody fusion (ALIF) device launched last July.
“We have been doing anterior...
K2M introduces Sahara AL expandable stabilisation system
K2M has launched the Sahara AL expandable stabilisation system, the company's first expandable product within its interbody portfolio. Sahara AL is the only lordotic...
Tiger Woods undergoes MIS ALIF for severe back and leg pain
World-renowned golfer Tiger Woods has announced on his website that he has undergone a minimally invasive anterior lumbar interbody fusion (MIS ALIF) procedure to...
Innovasis recieves FDA 510(k) clearance for PEEK standalone Ax ALIF System
Innovasis has become the first company to recieve US Food and Drug Administration (FDA) clearance for a standalone anterior lumbar interbody fusion (ALIF) system...
ChoiceSpine releases Harrier ALIF system
ChoiceSpine has launched Harrier, an anterior lumbar interbody fusion system. The device was cleared for marketing by the US Food and Drug Administration in...
SeaSpine launches Vu a.Pod prime nanometalene ALIF system
SeaSpine has begun a full commercial launch of its Vu a.Pod prime nanometalene system.
The system features a zero-profile, standalone anterior lumbar interbody device that...
ChoiceSpine acquires Exactech’s spine assets, launches Harrier ALIF system
Exactech has sold its spine assets to ChoiceSpine, as part of a “restructuring” and “divesture” move. Terms of the transaction were not released. The...
First clinical use of OrtoWay OrtoWell distractor tool successful
A German spine clinic has reported the successful application and ease of use of OrtoWay’s Ortowell for lateral minimally invasive fixation in a complicated...
Depuy Synthes Spine launches Synfix Evolution system
DePuy Synthes Spine has launched the Synfix Evolution system, a new implant for stand-alone anterior lumbar interbody fusion (ALIF). The Synfix Evolution system delivers...