Zimmer Biomet Acquiring LDR
Zimmer Biomet entered into a definitive agreement to acquire LDR for US $37/share in cash, for a transaction valued at ~$1.0BB with an expected 3Q16 close. Jun 07, 2016
Flower Orthopedics Launches Flower E-Kit And IndicationCube
Flower Orthopedics commenced full market launch of Flower E-Kit™, containing all required cannulated and plating instruments for midfoot, forefoot and ankle in one single-use package. Jun 07, 2016
NuVasive Acquiring Biotronic NeuroNetwork for $98 Million
NuVasive (NUVA) entered into a definitive agreement to acquire Biotronic NeuroNetwork, a U.S. provider of intraoperative neurophysiological monitoring services, for US $98MM in cash. Jun 06, 2016
Warning Letter Issued to Zimmer CAS
On 5/31/16, Zimmer Biomet received an FDA Warning Letter regarding observed non-conformities at the company’s Zimmer CAS/ORTHOsoft facility in Montreal, Quebec, Canada. Jun 06, 2016
First Implantations of Vertera Spine Porous PEEK COHERE Cervical Fusion Device
Vertera Spine announced first implantations with the COHERE™ Cervical Interbody Fusion system. Full market launch is expected in coming months. Jun 06, 2016
Initial Surgeries with LDR’s Titanium-coated ROI-C Cervical Cage
LDR announced initial implantations of the ROI-C® Titanium-Coated Cervical Cage. Jun 03, 2016
Life Spine’s Initial Cases and Multiple Surgeries with PLATEAU-Ti Spacer
Life Spine announced successful completion of initial cases with the PLATEAU®-Ti Spacer, a titanium interbody system featuring OSSEO-LOC™ surface treatment to support potential bone growth. Jun 02, 2016
Osseon Increases Independent Distribution Network
Osseon has increased its independent distribution network by 26% since January 2016, and is on track to expand its vertebral augmentation line with three new VCF products in the pipeline. Jun 02, 2016
Eden Spine’s CE Mark Approval for Thoracolumbar Plate
Eden Spine received CE Mark approval for the SPHYNX™ titanium plate to treat thoracolumbar instability. Jun 02, 2016
First Ray Receives FDA 510(k) Clearance for SpeedButton Soft Tissue Attachment System
First Ray received FDA 510(k) clearance to market the SpeedButton™ system for attachment of soft tissue to bone. Jun 02, 2016
