intervertebral body fusion
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Spine
Vy Spine Announces FDA Clearance for its ClariVy OsteoVy PEKK Cervical IBF
Tallahassee, FL., November 14, 2023 – OrthoSpineNews – Vy Spine, a spine innovation leader using differentiated materials and designs, announced…
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Spine
VySpine Announces FDA Clearance for UniVy OsteoVy-Ti Cervical IBF with NanoVy-HA
Tallahassee, FL — April 25, 2023 /OrthoSpineNews/ — VySpine, a spine innovation leader using differentiated materials and designs, announced today…
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Spine
VySpine Announces FDA Clearance for LumiVy Lumbar IBF with NanoVy Ti
Tallahassee, FL – January 17, 2023 /OrthoSpineNews/—VySpine, a spine innovation leader using differentiated materials and designs, announced today that it…
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Regulatory
joimax® Receives FDA Clearance to Market EndoLIF® Delta-Cage and DoubleWedge-Cage in the USA
September 7, 2021 KARLSRUHE, Germany–(BUSINESS WIRE)–German-based joimax®, the market leader in technologies and training methods for full-endoscopic and minimally invasive spinal…
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Spine
SeaSpine Launches Ventura(TM) NanoMetalene(R) Interbody Device
VISTA, Calif., Aug. 10, 2015 (GLOBE NEWSWIRE) — SeaSpine Holdings Corporation (NASDAQ:SPNE), a global medical technology company focused on surgical solutions for…
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Spine
New Stand-Alone Intervertebral Body Fusion Device Gets FDA Clearance
Surgeons treating patients with degenerative disc disease may now use a new stand-alone intervertebral body fusion device recently cleared by…
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