Stryker Spine announced FDA 510(k) clearance of Tritanium® PL, a highly-porous posterior lumbar cage manufactured via 3D additive manufacturing. Launch will occur in 2Q16.
DePuy Synthes entered into an exclusive strategic alliance with Value Stream Partners to facilitate customers’ implementation of bundled payment programs for hip and knee replacement.
Zimmer Biomet (ZBH) received FDA 510(k) clearance for compatibility of the Nexel™ Total Elbow with the Comprehensive® Segmental Revision System. This marks the 1st submission by ZBH to establish compatibility of two separate ZBH implant systems.
Brainlab introduced Auto-Knee, a new feature of traumaCad 2.5 that supports pre-op planning of knee arthroplasty by automatically registering anatomical landmarks.
EOS imaging entered into a co-promotion agreement whereby Stryker’s European Spine business will promote EOS imaging’s platform to existing and prospective customers in the U.K.