fixation
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Spine
SI-BONE, Inc. Announces First-In-Patient Procedures with FDA Breakthrough Device for Pelvic Fracture Fixation
SANTA CLARA, Calif., Oct. 10, 2024 (GLOBE NEWSWIRE) — SI-BONE, Inc. (Nasdaq: SIBN), a Silicon Valley-based medical device company dedicated…
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Spine
SI-BONE, Inc. Receives 510(k) Clearance and FDA Breakthrough Device Designation for Pelvic Fracture Fixation System
SANTA CLARA, Calif., Aug. 20, 2024 (GLOBE NEWSWIRE) — SI-BONE, Inc., (Nasdaq: SIBN), a Silicon Valley-based medical device company dedicated to…
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Spine
Accelus Introduces LineSider Modular-Cortical System for Posterior Fixation
Continued expansion of LineSider Spinal System portfolio offers surgeons increased visibility and versatility PALM BEACH GARDENS, Fla., Jan. 29, 2024…
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Regulatory
Spineway-VEOS FDA 510(k) clearance
Spineway obtains 510(k) clearance from the FDAfor its VEOS spinal fixation system Ecully, October 19, 2023- Spineway Group, a specialist…
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