DePuy Synthes Spine launched the ZERO-P NATURAL™ Plate, designed for use with the CC Natural allograft spacer, for spinal fusion procedures in the neck.
Results from a pre-clinical interbody fusion study of Stryker Spine’s 3D-printed Tritanium PL Interbody Cage demonstrated statistically superior range of motion, bone in-growth and greater average construct stiffness vs. PEEK and titanium plasma-sprayed PEEK cages.
Zimmer Biomet acquired RespondWell® telerehabilitation technology, designed to provide personalized, clinician-supervised post-surgical physical therapy in a patient’s home.
Seven-year outcomes study data demonstrated statistical superiority of Zimmer Biomet’s Mobi-C® Cervical Disc vs. 2-level ACDF in overall success.Â
NuVasive received FDA clearance for magnetic resonance imaging under certain conditions on patients treated with the MAGEC® growth modulation system.
BONESUPPORT raised SEK 327MM (~US $37MM). Funds will support clinical data collection, product pipeline development and expansion of CERAMENT sales in existing and new markets.
SeaSpine received FDA 510(k) clearance to market the Shoreline™ ACS Anterior Cervical Standalone system. Full commercial launch is slated for 1H17.