cervical
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Spine
NGMedical GmbH Announces First Cases in the USA of its AM Titanium Cervical Interbody BEE®
September 9, 2021 NONNWEILER, Germany & SCOTTSDALE, Ariz.–(BUSINESS WIRE)–NGMedical, a German medical device manufacturer exclusively focused on creating innovative technologies…
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Regulatory
Intelivation Technologies received FDA approval for the Advantage-C™ PEEK Cervical Interbody Fusion device
–Saint Simons Island, GA, September 8, 2021 /OrthoSpineNews/: Intelivation Technologies, a medical device company with a growing product portfolio announced…
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Spine
ADR Innovator Dr. Todd Lanman Becomes First in U.S. to Perform Reversal of Prior 3-Level Cervical Fusion
(LOS ANGELES) – SEPT. 2021 – Leading artificial disc replacement innovator Dr. Todd H. Lanman, founder of the national ADR Advanced…
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Regulatory
Aurora Spine Corporation Announces FDA 510(k) Clearance for DEXA-C™ Cervical Interbody System
Product approval is the first in the world using Company’s proprietary and patented DEXA Technology™ for custom made implants based…
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Biologics
Bioventus Launches OSTEOAMP® SELECT Flowable Nationwide
DURHAM, N.C., July 13, 2021 (GLOBE NEWSWIRE) — Bioventus Inc. (Nasdaq: BVS) (“Bioventus” or the “Company”), a global leader in innovations for…
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Neuro
ADR Spinal Restoration Center Opens Up 2-Level prodisc® and 1-Level Synergy Disc® Clinical Trials in Los Angeles
LOS ANGELES (PRWEB) MAY 21, 2021 Those suffering from painful degenerative or herniated discs in their necks might find relief in…
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Regulatory
ChoiceSpine™ Announces FDA Clearance and Clinical Use of Blackhawk™ Ti Cervical Spacer System
May 25, 2021 KNOXVILLE, Tenn.–(BUSINESS WIRE)–ChoiceSpine LLC, a privately held spinal device manufacturer based in Knoxville, TN, announced today that…
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Regulatory
MCRA CRO Assists Simplify Medical, Recently Acquired by NuVasive, on FDA-Approval for Two Level use of its Cervical Disc
– MCRA’s CRO assisted Simplify Medical, Inc. (Simplify Medical) with the conduct, execution and oversight of the clinical study, including…
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Regulatory
NuVasive’s Simplify Disc Receives FDA Approval for Two-Level Cervical Total Disc Replacement
Simplify® Cervical Artificial Disc achieved the highest overall clinical success rate at both one- and two-levels compared to any other…
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Regulatory
Orthofix Announces FDA Clearance and Initial Patient Implant of the Company’s First 3D-Printed Titanium Cervical Spacer System with Nanovate Technology
April 5, 2021 LEWISVILLE, Texas–(BUSINESS WIRE)–Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company with a spine and extremities focus,…
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Regulatory
Aurora Spine Receives FDA 510(K) Clearance for Its Proprietary APOLLO Anterior Cervical Plate
CARLSBAD, Calif., March 25, 2021 (GLOBE NEWSWIRE) — Aurora Spine Corporation (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF),…
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Spine
ATEC Furthers Clinical Distinction with Launch of InVictus® OCT Posterior Fixation System for the Cervical and Thoracic Spine
Completes InVictus System Allowing Seamless Spinal Fixation from Occiput to Ilium CARLSBAD, Calif., March 15, 2021 (GLOBE NEWSWIRE) — Alphatec…
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Regulatory
NGMedical GmbH Receives FDA Clearance for Its AM Titanium Cervical Interbody BEE®
NGMedical achieves milestone with first FDA clearance for its innovative spinal implants. SCOTTSDALE, Ariz., February 3, 2021 (Newswire.com) – NGMedical, a…
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Regulatory
icotec ag Announces the Market Launch of its BlackArmor® Anterior Cervical Plate in the United States
ALTSTAETTEN, Switzerland, Jan. 28, 2021 /PRNewswire/ — icotec ag, a leading medical device manufacture of BlackArmor® Carbon/PEEK implants, announces the United States market release of the…
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Regulatory
ChoiceSpine™ Announces Line Extension of Tiger Shark™ Cervical Spacer System
January 25, 2021 KNOXVILLE, Tenn.–(BUSINESS WIRE)–ChoiceSpine LLC, a privately held spinal device manufacturer based in Knoxville, TN, announced today that…
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