Spine

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

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

Strategic orthopaedic-related 510(k)s issued in July 2017 include: EIT Cellular Titanium Cages (EIT Emerging Implant Technologies), Lumbar Interbody System (HD LifeSciences),...

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

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

Expanding Orthopedics was granted two additional U.S. Patents covering expandable interbody cage technology....

Renovis Surgical received FDA 510(k) clearance to market Tesera® 3D-printed posterior lumbar interbody fusion systems....

Xtant Medical received FDA 510(k) clearance for additional sizes of Calix-C™ cervical interbody cages, as well as use of the...

Life Spine announced the first clinical uses of TiBOW™, its minimally invasive expandable TLIF system featuring Osseo-Loc™ surface technology....

ApiFix received regulatory approval to market the ApiFix system in Australia to treat Adolescent Idiopathic Scoliosis....