Media Release Medacta Announces FDA Clearance for Mecta-C Stand Alone Anterior Cervical Interbody Fusion Device CASTEL SAN PIETRO, 06 March 2020 - Medacta is proud to announce the clearance from the U.S. Food and Drug Administration (FDA) for the Mecta-C Stand Alone platform for anterior cervical discectomy and fusion procedures (ACDF). Mecta-C Stand Alone is indicated for use from C2 to T1 in skeletally mature patients suffering from degenerative disc disease. The platform incorporates the benefits of an anterior plate with a versatile screw system, thus requiring no additional fixation. The modular design is an important characteristic of the Mecta-C Stand Alone system, allowing the surgeon to intraoperatively select four plating options - Flush, Trio, Hybrid and Quattro - to best treat various patient needs and anatomies. Each option allows for either a locking screw or lag screw feature, and includes an easy-to-use locking mechanism that provides surgeons with unique intraoperative versatility. The Mecta-C Stand Alone anterior cervical interbody fusion devices are offered in TiPEEK, Medacta's plasma-sprayed titanium coating that provides an added value to improve stability and increase the migration resistance. Mecta-C Stand Alone is an indication-specific interbody fusion device which enriches the suite of 360° cervical solutions to provide a treatment to numerous cervical spine disorders. For more information on Medacta Spine visit spine.medacta.com. Contact Issuer: Medacta Group SA Key word(s): Health
End of Corporate News |
Language: | English |
Company: | Medacta Group SA |
Strada Regina | |
6874 Castel San Pietro | |
Switzerland | |
Phone: | +41 91 696 6060 |
E-mail: | info@medacta.ch, investor.relations@medacta.ch |
Internet: | www.medacta.com |
ISIN: | CH0468525222 |
Listed: | SIX Swiss Exchange |
EQS News ID: | 991689 |
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991689 06.03.2020