NuVasive entered into a definitive agreement to acquire Mega Surgical, its exclusive distributor in Brazil. The transaction is expected to close within 1Q16.
FDA has accepted for filing Vericel’s BLA for MACI™, matrix-applied characterized autologous cultured chondrocytes intended to treat adult symptomatic knee cartilage defects.
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.Â
Zimmer Biomet (ZBH) received FDA 510(k) clearance for compatibility of the Nexelâ„¢ Total Elbow with the Comprehensive® Segmental Revision System. This marks the 1st submission by ZBH to establish compatibility of two separate ZBH implant systems.Â
Brainlab introduced Auto-Knee, a new feature of traumaCad 2.5 that supports pre-op planning of knee arthroplasty by automatically registering anatomical landmarks.