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Cresco Spine Receives FDA 510(k) Clearance for the Spring Distraction System (SDS™) – Ortho Spine News
19-01-2026 Schiedam, The Netherlands – OrthoSpineNews – Cresco Spine today announced that the U.S. Food and Drug Administration has granted 510(k) clearance for the Spring Distraction System (SDSTM), a dynamic, growth-friendly implant for the treatment of early onset scoliosis. Earlier in its regulatory trajectory, SDSTM received FDA Breakthrough Device Designation. Since the introduction of this program in 2015, fewer than 0.1 percent of all dev
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1 Articles
Cresco Spine Receives FDA 510(k) Clearance for the Spring Distraction System (SDS™) – Ortho Spine News
19-01-2026 Schiedam, The Netherlands – OrthoSpineNews – Cresco Spine today announced that the U.S. Food and Drug Administration has granted 510(k) clearance for the Spring Distraction System (SDSTM), a dynamic, growth-friendly implant for the treatment of early onset scoliosis. Earlier in its regulatory trajectory, SDSTM received FDA Breakthrough Device Designation. Since the introduction of this program in 2015, fewer than 0.1 percent of all dev
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