FDA 510(k)

TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System

N.º K: K231504 · 2023-09-11

Fecha de decisión2023-09-11

Código de productoHWC

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Vilex, LLC. It received FDA 510(k) clearance on 2023-09-11 under 510(k) number K231504. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System?

TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System is a medical device that received FDA 510(k) clearance on 2023-09-11. The listed applicant is Vilex, LLC. The 510(k) number is K231504.

When did TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System receive FDA 510(k) clearance?

TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System received FDA 510(k) clearance on 2023-09-11, under 510(k) number K231504.

Who is the listed applicant for TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System?

The FDA 510(k) record lists Vilex, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System?

The FDA product code for TITANEX™ MICROBEAM Screw System, TITANEX™ ARTEMIS Screw System is HWC. This falls under the Cardiovascular category.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Otros registros que enlistan a Vilex, LLC como solicitante

K260900DYNEX® External Fixation Systems K250304TITANEX Screw Systems K240475Hintermann Series H2 Total Ankle System K243408TACTIX Vector Syndesmosis System K233816Sistema de Plaqueo Charcot REDEMPTION K240035TACTIX Vector Syndesmosis System

Ver todos los 17 dispositivos →

Dispositivos relacionados (Código: HWC)

K262975Sistema Arthrex BeamingArthrex, Inc.K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps Ortho K261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower Orthoped K262344Large Compression ScrewsTriMed, Inc.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.