cervical
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Spine
Providence Medical Technology Announces Completion of Enrollment in the FUSE Clinical Study for High-Risk Cervical Fusion Patients
PLEASANTON, Calif., May 11, 2023 /PRNewswire/ — Providence Medical Technology, Inc. (PMT), a leader in medical device innovation for spine surgery, today…
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Spine
Centinel Spine® Announces Record Revenue and Growth in 2022, Achieving Number Two Market Position in Cervical and Lumbar Total Disc Replacement
Full year 2022 Motion Preservation record revenue was approximately $45 million, achieving the number two total disc replacement (TDR) market position…
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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
IMPLANET Receives FDA Clearance for Its Squale™ Anterior Cervical Cage Range
April 11, 2023 BORDEAUX, France & BOSTON–(BUSINESS WIRE)–Regulatory News: IMPLANET (Euronext Growth: ALIMP, FR0013470168, eligible for PEA-PME equity savings plans)…
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Spine
ZSFab Announces Second Clinical Use of the ZSFab Cervical Interbody System for ACDF
WALTHAM, Mass., April 10, 2023 (GLOBE NEWSWIRE) — ZSFab, Inc., a 3D-printing medical device company, is pleased to announce that…
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Spine
ZSFab Announces First US Clinical Use of ZSFab Cervical Interbody System for ACDF
WALTHAM, Mass., April 05, 2023 (GLOBE NEWSWIRE) — ZSFab, Inc., a 3D-printing medical device company, is proud to announce that…
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Spine
Aurora Spine Receives IRB Multi-Site Selection Approval for its DEXA-C™ Cervical Interbody System
Carlsbad, Calif., April 04, 2023 (GLOBE NEWSWIRE) — Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV:ASG) (OTCQB:ASAPF), a designer…
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Spine
Aurora Spine Receives IRB Approval To Commence Multicenter Study for its DEXA-C™ Cervical Interbody System
CARLSBAD, Calif., March 02, 2023 (GLOBE NEWSWIRE) — Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF),…
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Spine
NuVasive Enhances C360 Portfolio with Expanded Indications for Modulus Cervical and Attrax Putty
Attrax Putty is now on-label for use with cervical Modulus interbody implants SAN DIEGO, Feb. 21, 2023 /PRNewswire/ — NuVasive, Inc. (NASDAQ: NUVA), the…
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Spine
Curiteva Inc. Announces FDA 510(k) Clearance for Inspire 3D Porous PEEK HAFUSE Cervical Interbody System
Huntsville, AL based technology company, Curiteva announces the first FDA 510(k) cleared 3D printed PEEK implant, the Inspire Porous PEEK…
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Regulatory
NanoHive Medical, LLC Receives FDA 510(k) Clearance for Hive™ Standalone Cervical System
NanoHive’s New Hive Zero Profile Standalone Cervical Cage Boston, MA, January 9, 2023 /OrthoSpineNews/ – NanoHive Medical has received 510(k)…
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Spine
Centinel Spine® Announces First Commercial Use of prodisc® C SK Cervical Total Disc Replacement Product
prodisc® C SK expands availability of Centinel Spine’s portfolio of FDA-approved cervical total disc replacement (TDR) devices.Centinel Spine now has…
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Spine
Centinel Spine Wins Third Consecutive Spine Technology Award for prodisc® Cervical Portfolio & Match-the-Disc Platform
Centinel Spine wins Best New Technology Award for its prodisc® Cervical Portfolio & Match-the-Disc Platformprodisc portfolio includes four total disc replacement devices…
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Spine
Drs. Todd H. Lanman and Jason M. Cuellar Become First Surgeons in the U.S. to Perform 3-Level ADR With Prodisc® C Vivo
Todd H. Lanman, MD, and Jason M. Cuellar, MD, Ph.D., restore spinal motion in a woman with 4-level disc degeneration…
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Spine
ulrich Medical USA™ Receives 510(k) Clearance for Flux-C™ 3D Printed Porous Titanium Cervical Interbody Prior to NASS
ST. LOUIS, Oct. 14, 2022 /PRNewswire/ — ulrich medical USA, Inc., a privately held medical device company focused on developing and commercializing musculoskeletal…
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