Life Spine Performs Cases with Multiple Methods of In Situ Expansion

Life Spine announced the first cases performed using multiple methods of in situ expansion with the PROLIFT® Lordotic system and the TiBOW™ Expandable TLIF Spacer.

CoreLink Launches Stackable Guide Wire for Entasis SI Joint Fusion

CoreLink introduced Scaltoff™, a stackable guide wire for the Entasis® Sacroiliac Joint Fusion system.

Stryker Spine Receives FDA 510(k) Clearance for Serrato Pedicle Screw

Stryker Spine received FDA 510(k) clearance to market the Serrato™ Pedicle Screw.

Strategic Orthopaedic-related 510(k)s Issued in July 2017: Interbody Focus

Strategic orthopaedic-related 510(k)s issued in July 2017 include: EIT Cellular Titanium Cages (EIT Emerging Implant Technologies), Lumbar Interbody System (HD LifeSciences), Gemini-C Hybrid Cervical Interbody System (Osseus Fusion Systems), LumFuse-TP (Precifit Medical), Anchorman Tibial Ligament Fixation (Summit Medical)

Camber Spine Commences U.S. Launch of SPIRA Open Matrix ALIF

Camber Spine Technologies received FDA 510(k) clearance and commenced U.S. launch of the SPIRA™ Open Matrix ALIF device, manufactured with additive techniques. 

Spine Wave Launches Proficient Posterior Cervical System

Spine Wave commenced limited market release of the Proficient® Posterior Cervical system. Full launch is slated for early 4Q17.