Life Spine Gains FDA Clearance for PRO-LINK Ti Stand-Alone Cervical Spacer
Life Spine received FDA 510(k) clearance to market additional indications for the PRO-LINK® Ti Stand-Alone Cervical Spacer. May 23, 2018
Wenzel Spine Announces Case Study of VariLift-LX System
Wenzel Spine announced publication of a case series detailing endoscopic transforaminal decompression and fusion with the VariLift-LX system. May 23, 2018
Zimmer Biomet Gains 510(k) Clearance for Zyston Strut Open Titanium Interbody Spacer
Zimmer Biomet received FDA 510(k) clearance to market the Zyston® Strut Open Titanium Interbody Spacer, the company's first 3D-printed titanium spinal implant. May 23, 2018
CrossRoad Extremity Launching Active Stabilization MPJ Implant
CrossRoads Extremity Systems received FDA clearance to market the DynaFORCE® Active Stabilization MPJ Implant. May 23, 2018
In’Tech Medical to Acquire Bradshaw Medical
In™Tech Medical, a contract manufacturer for the orthopaedic industry, entered into a binding agreement to acquire Bradshaw Medical. May 23, 2018
Episurf Medical to Gain Another EU Patent
Episurf Medical will be granted approval for an EU patent addressing a drill guide for use with the Episealer® Femoral Twin implant. May 22, 2018
NuVasive’s PRECICE STRYDE Limb Lengthening System Used in First Surgery
NuVasive announced the first surgery performed with PRECICE STRYDE limb lengthening system. Limited launch is slated for mid-2018. May 22, 2018
DePuy Synthes Introduces GLOBAL UNITE Reverse Fracture Shoulder
DePuy Synthes launched the GLOBAL UNITE Reverse Fracture Shoulder for use in patients with a deficient rotator cuff. May 22, 2018
Cerapedics Study Results: i-FACTOR Bone Graft in Lumbar Posterolateral Spine
Study results indicate that Cerapedics' i-FACTOR Peptide Enhanced Bone Graft demonstrated a 50% fusion rate in lumbar posterolateral spine surgery patients vs. 20% fusion rate with allograft. May 22, 2018
Providence Medical Technology Gains FDA Clearance for DTRAX Spinal System
Providence Medical Technology announced FDA 510(k) clearance to market its DTRAX® system for use in posterior cervical fusion. May 22, 2018
