Carlsbad, Calif.-based Aurora Spine has received FDA 510(k) clearance for TiNano spinal fusion implant.
Minneapolis-based Zimmer Spine will now market its Puros demineralized bone matrix block and strip in the U.S.
Atlanta-based MedShape received FDA 510(k) clearance for the ExoShape Femoral Soft Tissue Fastener for anterior cruciate ligament repair.
Columbia, Md.-based ACell launched its MatriStem Multilayer Wound Matrix for deep, hard-to-heal wounds.
Irvine, Calif.-based Interventional Spine received FDA clearance for 11 additional sizes of its Opticage Expandable Interbody Fusion Device.
BioStructures announced the U.S. Food and Drug Administration granted 510(k) clearance for Signafuse Bioactive Bone Graft Putty.
Benvenue Medical received 510(k) clearance from the U.S. Food and Drug Administration for its Kiva VCF system to treat vertebral compression fractures.
IMRIS announced the initial launch of the world's first Magnetic Resonance-safe and Computed Tomography-compatible horseshoe headrest for the positioning of patients during neurosurgical procedures requiring intraoperative imaging in the VISIUS Surgical Theatre.
Smith & Nephew announced the U.S. launch of its POLARSTEM cementless stem for total hip replacement.
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