screw
-
Extremities
Forma Medical Announces Milestone Achievement: 15th Patient Successfully Treated with OptimalMTP®, the World’s First Minimally Invasive Plate and Screw System
CAMP HILL, Pa., September 5, 2024–(BUSINESS WIRE)–Forma Medical Inc., a leader in innovative orthopedic solutions, proudly announces the successful treatment…
Read More » -
Extremities
Bioretec reports successful clinical outcomes from U.S. controlled launch of RemeOs™ trauma screw: fracture healing confirmed in 100% of surgical procedures
TAMPERE, Finland, June 19, 2024 /PRNewswire/ — Bioretec Ltd., a pioneer in biodegradable orthopedic implants, is pleased to announce that a number of…
Read More » -
Extremities
Tyber Medical Receives FDA Clearance on Plating System Line Extension
Tyber Medical Broadens Its Vast Plating Portfolio with FDA Approval of Additional Screw and Plate Options, and Indications for Mini-Frag…
Read More » -
Biologics
TheraCell Exceeds Expectations With Its Limited Launch Of The TheraFuze DBF® Fiber Anchor™
TheraCell has surpassed 200 Fiber Anchors implanted, providing surgeons a solution for improved screw fixation July 6, 2021 LOS ANGELES, July…
Read More » -
Robotics
Globus Medical Announces First Surgeries with Revolutionary CREO ONE™ Robotic Screw
The Latest Enhancement to Robotically Navigated Spine Surgery with ExcelsiusGPS® AUDUBON, Pa., April 15, 2021 (GLOBE NEWSWIRE) — Globus Medical, Inc. (NYSE:…
Read More » -
Extremities
OSSIO Announces U.S. Launch and First Commercial Use of the Bio-Integrative OSSIOfiber®Compression Screw Portfolio
Company Secures $20 Million in Financing to Accelerate Product Development & Advance Commercialization WOBURN, Mass. – OSSIO, Inc., an orthopedic…
Read More » -
Spine
TheraCell Announces First Surgical Use Of TheraFuze DBF® Fiber Anchor™ For Pedicle Screw Augmentation
LOS ANGELES, Nov. 3, 2020 /PRNewswire/ — TheraCell Inc., a leading bone technology company today announced that it has completed the first three spine surgical…
Read More » -
Extremities
Acuitive Technologies Granted FDA 510(k) Clearance for CITREGEN™ CITRELOCK™ Tendon Interference Screw System
ALLENDALE, N.J., Oct. 21, 2020 /PRNewswire/ — Acuitive Technologies today announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the CITRELOCK™ Interference Screw System…
Read More »