FDA 510(k) Clearance
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Biologics
Ventris Medical Receives 510(k) Clearance for Amplify® Standalone Bone Graft Putty and Bone Graft Extender
NEWPORT BEACH, Calif., Sept. 14, 2022 /PRNewswire/ — Ventris Medical, a privately held orthobiologics and tissue regeneration company, today announced that the…
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Spine
NeuraMedica Inc. Receives FDA 510(k) Clearance for DuraFuse Dural Clips for Fast & Secure Dural Closure
Oregon City, Oregon, August 31, 2022 /OrthoSpineNews/ – NeuraMedica Inc., a medical device company developing innovative products for neurosurgery, has…
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Regulatory
Point Robotics Receives FDA 510(k) Clearance for its Point™ Kinguide Robotic-Assisted Surgical System to Push the Boundaries of Precision Spinal Surgeries
August 23, 2022 – Point Robotics MedTech Inc., /OrthoSpineNews/ – (Point Robotics), a rising leader in the field of minimal…
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Regulatory
Medtronic receives FDA clearance for next-generation UNiD™ Spine Analyzer with degenerative spine surgery predictive model
Powered by a database of over 10,000 surgical cases, Medtronic continues to evolve the UNiD™ platform to help surgeons plan…
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Spine
Cutting Edge Spine Announces FDA 510(k) Clearance of T-FIX 3DSI Joint Fusion System with Proprietary Trabecular Technology
The T-FIX 3DSI Joint Fusion System is the first of many systems from Cutting Edge Spine to implement proprietary trabecular…
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