Onkos Surgical received FDA 510(k) clearance to market the ELEOS™ Limb Salvage System to treat bone loss due to cancer, trauma or previous surgical procedures. Full launch is slated for 1Q17.
DePuy Synthes announced the availability of Expert Tibial Nail PROtect, featuring a resorbable antibiotic coating designed to provide protection from bacterial colonization in patients at high risk of infection.Â
General Electric reached an agreement to acquire a 75% stake in Concept Laser, manufacturer of powder bed-based laser additive manufacturing machines, for 549MM (~US $599MM).Â
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.
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.
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